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Motor Neurone Disease v0.36 Bryony Thompson Panel types changed to Victorian Clinical Genetics Services; Royal Melbourne Hospital; Rare Disease
Motor Neurone Disease v0.35 UBQLN4 Bryony Thompson Classified gene: UBQLN4 as Amber List (moderate evidence)
Motor Neurone Disease v0.35 UBQLN4 Bryony Thompson Gene: ubqln4 has been classified as Amber List (Moderate Evidence).
Motor Neurone Disease v0.34 UBQLN4 Bryony Thompson gene: UBQLN4 was added
gene: UBQLN4 was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: UBQLN4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: UBQLN4 were set to 28463112; 30804504
Phenotypes for gene: UBQLN4 were set to Amyotrophic lateral sclerosis
Review for gene: UBQLN4 was set to AMBER
Added comment: A single familial case and supporting functional studies and animal model.
Sources: Expert list
Mendeliome v0.1885 HSPB3 Zornitza Stark Marked gene: HSPB3 as ready
Mendeliome v0.1885 HSPB3 Zornitza Stark Gene: hspb3 has been classified as Red List (Low Evidence).
Mendeliome v0.1885 HSPB3 Zornitza Stark Phenotypes for gene: HSPB3 were changed from to Neuronopathy, distal hereditary motor, type IIC, MIM# 613376
Mendeliome v0.1884 HSPB3 Zornitza Stark Publications for gene: HSPB3 were set to
Mendeliome v0.1883 HSPB3 Zornitza Stark Mode of inheritance for gene: HSPB3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1882 HSPB3 Zornitza Stark Classified gene: HSPB3 as Red List (low evidence)
Mendeliome v0.1882 HSPB3 Zornitza Stark Gene: hspb3 has been classified as Red List (Low Evidence).
Mendeliome v0.1881 HSPB3 Zornitza Stark reviewed gene: HSPB3: Rating: RED; Mode of pathogenicity: None; Publications: 20142617, 27549087; Phenotypes: Neuronopathy, distal hereditary motor, type IIC, MIM# 613376; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary Neuropathy_CMT - isolated v0.15 HSPB3 Zornitza Stark Marked gene: HSPB3 as ready
Hereditary Neuropathy_CMT - isolated v0.15 HSPB3 Zornitza Stark Gene: hspb3 has been classified as Red List (Low Evidence).
Hereditary Neuropathy_CMT - isolated v0.15 HSPB3 Zornitza Stark Publications for gene: HSPB3 were set to
Hereditary Neuropathy_CMT - isolated v0.14 HSPB3 Zornitza Stark Classified gene: HSPB3 as Red List (low evidence)
Hereditary Neuropathy_CMT - isolated v0.14 HSPB3 Zornitza Stark Gene: hspb3 has been classified as Red List (Low Evidence).
Hereditary Neuropathy_CMT - isolated v0.13 HSPB3 Zornitza Stark reviewed gene: HSPB3: Rating: RED; Mode of pathogenicity: None; Publications: 20142617, 27549087; Phenotypes: Neuronopathy, distal hereditary motor, type IIC, MIM# 613376; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary Neuropathy - complex v0.37 GJC2 Zornitza Stark Marked gene: GJC2 as ready
Hereditary Neuropathy - complex v0.37 GJC2 Zornitza Stark Gene: gjc2 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.37 GJC2 Zornitza Stark Classified gene: GJC2 as Green List (high evidence)
Hereditary Neuropathy - complex v0.37 GJC2 Zornitza Stark Gene: gjc2 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.36 GJC2 Zornitza Stark gene: GJC2 was added
gene: GJC2 was added to Hereditary Neuropathy - complex. Sources: NHS GMS
Mode of inheritance for gene: GJC2 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: GJC2 were set to Leukodystrophy, hypomyelinating, 2, MIM# 608804
Review for gene: GJC2 was set to GREEN
Added comment: Demyelinating neuropathy; axonal sensory neuropathy.
Sources: NHS GMS
Hereditary Neuropathy - complex v0.35 FXN Zornitza Stark Marked gene: FXN as ready
Hereditary Neuropathy - complex v0.35 FXN Zornitza Stark Gene: fxn has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.35 FXN Zornitza Stark Tag STR tag was added to gene: FXN.
Hereditary Neuropathy - complex v0.35 FXN Zornitza Stark Classified gene: FXN as Green List (high evidence)
Hereditary Neuropathy - complex v0.35 FXN Zornitza Stark Gene: fxn has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.34 FXN Zornitza Stark gene: FXN was added
gene: FXN was added to Hereditary Neuropathy - complex. Sources: NHS GMS
Mode of inheritance for gene: FXN was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: FXN were set to Friedreich ataxia, MIM# 229300
Mode of pathogenicity for gene: FXN was set to Other
Review for gene: FXN was set to GREEN
Added comment: Peripheral sensory neuropathy is part of the phenotype. Note only ~2% of cases are due to SNVs, majority due to STRs.
Sources: NHS GMS
Motor Neurone Disease v0.33 TIA1 Bryony Thompson Marked gene: TIA1 as ready
Motor Neurone Disease v0.33 TIA1 Bryony Thompson Gene: tia1 has been classified as Amber List (Moderate Evidence).
Motor Neurone Disease v0.33 TIA1 Bryony Thompson Classified gene: TIA1 as Amber List (moderate evidence)
Motor Neurone Disease v0.33 TIA1 Bryony Thompson Gene: tia1 has been classified as Amber List (Moderate Evidence).
Motor Neurone Disease v0.32 TIA1 Bryony Thompson gene: TIA1 was added
gene: TIA1 was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: TIA1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: TIA1 were set to 29235362; 29886022; 29773329; 29699721; 29216908; 24659297; 29457785; 28817800
Review for gene: TIA1 was set to AMBER
Added comment: >3 cases with ALS and functional studies, but no true replication study
Sources: Expert list
Motor Neurone Disease v0.31 TAF15 Bryony Thompson Marked gene: TAF15 as ready
Motor Neurone Disease v0.31 TAF15 Bryony Thompson Gene: taf15 has been classified as Amber List (Moderate Evidence).
Motor Neurone Disease v0.31 TAF15 Bryony Thompson Classified gene: TAF15 as Amber List (moderate evidence)
Motor Neurone Disease v0.31 TAF15 Bryony Thompson Gene: taf15 has been classified as Amber List (Moderate Evidence).
Motor Neurone Disease v0.30 TAF15 Bryony Thompson gene: TAF15 was added
gene: TAF15 was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: TAF15 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: TAF15 were set to 21438137; 22065782; 27810362; 28889094
Phenotypes for gene: TAF15 were set to Amyotrophic lateral sclerosis
Review for gene: TAF15 was set to AMBER
Added comment: No family studies, but >3 cases and functional studies.
Sources: Expert list
Motor Neurone Disease v0.29 UBA1 Bryony Thompson Deleted their review
Motor Neurone Disease v0.29 SS18L1 Bryony Thompson Marked gene: SS18L1 as ready
Motor Neurone Disease v0.29 SS18L1 Bryony Thompson Gene: ss18l1 has been classified as Green List (High Evidence).
Motor Neurone Disease v0.29 SS18L1 Bryony Thompson Classified gene: SS18L1 as Green List (high evidence)
Motor Neurone Disease v0.29 SS18L1 Bryony Thompson Gene: ss18l1 has been classified as Green List (High Evidence).
Motor Neurone Disease v0.28 TRIP4 Bryony Thompson Deleted their review
Motor Neurone Disease v0.28 SS18L1 Bryony Thompson gene: SS18L1 was added
gene: SS18L1 was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: SS18L1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SS18L1 were set to 25888396; 24360741; 23708140; 30976389
Phenotypes for gene: SS18L1 were set to amyotrophic lateral sclerosis
Review for gene: SS18L1 was set to GREEN
Added comment: >3 cases with heterozygote variants (de novo status confirmed or expected), and supporting functional evidence.
Sources: Expert list
Mendeliome v0.1881 FBXO38 Zornitza Stark Marked gene: FBXO38 as ready
Mendeliome v0.1881 FBXO38 Zornitza Stark Gene: fbxo38 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1881 FBXO38 Zornitza Stark Phenotypes for gene: FBXO38 were changed from to Neuropathy, distal hereditary motor, type IID, 615575; dHMN/dSMA
Mendeliome v0.1880 FBXO38 Zornitza Stark Publications for gene: FBXO38 were set to
Mendeliome v0.1879 FBXO38 Zornitza Stark Mode of inheritance for gene: FBXO38 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mendeliome v0.1878 FBXO38 Zornitza Stark Classified gene: FBXO38 as Amber List (moderate evidence)
Mendeliome v0.1878 FBXO38 Zornitza Stark Gene: fbxo38 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1877 FBXO38 Zornitza Stark reviewed gene: FBXO38: Rating: AMBER; Mode of pathogenicity: None; Publications: 24207122, 31420593; Phenotypes: Neuronopathy, distal hereditary motor, type IID, 615575, dHMN/dSMA; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Hereditary Neuropathy_CMT - isolated v0.13 FBXO38 Zornitza Stark Marked gene: FBXO38 as ready
Hereditary Neuropathy_CMT - isolated v0.13 FBXO38 Zornitza Stark Gene: fbxo38 has been classified as Amber List (Moderate Evidence).
Hereditary Neuropathy_CMT - isolated v0.13 FBXO38 Zornitza Stark Classified gene: FBXO38 as Amber List (moderate evidence)
Hereditary Neuropathy_CMT - isolated v0.13 FBXO38 Zornitza Stark Gene: fbxo38 has been classified as Amber List (Moderate Evidence).
Hereditary Neuropathy_CMT - isolated v0.12 FBXO38 Zornitza Stark reviewed gene: FBXO38: Rating: AMBER; Mode of pathogenicity: None; Publications: 24207122, 31420593; Phenotypes: Neuronopathy, distal hereditary motor, type IID, MIM# 615575; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Hereditary Neuropathy - complex v0.33 FAH Zornitza Stark Marked gene: FAH as ready
Hereditary Neuropathy - complex v0.33 FAH Zornitza Stark Gene: fah has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.33 FAH Zornitza Stark Classified gene: FAH as Green List (high evidence)
Hereditary Neuropathy - complex v0.33 FAH Zornitza Stark Gene: fah has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.32 FAH Zornitza Stark gene: FAH was added
gene: FAH was added to Hereditary Neuropathy - complex. Sources: NHS GMS
Mode of inheritance for gene: FAH was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: FAH were set to Tyrosinemia, type I, MIM# 276700
Review for gene: FAH was set to GREEN
Added comment: Episodic peripheral neuropathy.
Sources: NHS GMS
Motor Neurone Disease v0.27 PRPH Bryony Thompson Classified gene: PRPH as Amber List (moderate evidence)
Motor Neurone Disease v0.27 PRPH Bryony Thompson Gene: prph has been classified as Amber List (Moderate Evidence).
Motor Neurone Disease v0.26 PRPH Bryony Thompson changed review comment from: Reported in OMIM as an ALS susceptibility loci. Two heterozygous cases and a homozygous case reported, with some supporting evidence in a mouse model.
Sources: Expert list; to: Reported in OMIM as an ALS susceptibility loci. Two heterozygous cases and a homozygous case (Asp141Tyr) reported that doesn't appear to have more severe disease. The Asp141Tyr missense NFE AF in gnomAD is 0.005730, which is on the high side. There is also some supporting evidence in a mouse model.
Sources: Expert list
Motor Neurone Disease v0.26 PRPH Bryony Thompson changed review comment from: ALS susceptibility loci
Sources: Expert list; to: Reported in OMIM as an ALS susceptibility loci. Two heterozygous cases and a homozygous case reported, with some supporting evidence in a mouse model.
Sources: Expert list
Motor Neurone Disease v0.26 PRPH Bryony Thompson edited their review of gene: PRPH: Changed publications: 20363051, 15322088, 15446584
Mendeliome v0.1877 DRP2 Zornitza Stark Marked gene: DRP2 as ready
Mendeliome v0.1877 DRP2 Zornitza Stark Gene: drp2 has been classified as Green List (High Evidence).
Mendeliome v0.1877 DRP2 Zornitza Stark Classified gene: DRP2 as Green List (high evidence)
Mendeliome v0.1877 DRP2 Zornitza Stark Gene: drp2 has been classified as Green List (High Evidence).
Mendeliome v0.1876 DRP2 Zornitza Stark gene: DRP2 was added
gene: DRP2 was added to Mendeliome. Sources: Expert list
Mode of inheritance for gene: DRP2 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Publications for gene: DRP2 were set to 26227883; 11430802; 31217940; 22764250; 29473052
Phenotypes for gene: DRP2 were set to Charcot Marie Tooth, intermediate X-linked; HMSN
Review for gene: DRP2 was set to GREEN
Added comment: Three unrelated families, functional data.
Sources: Expert list
Hereditary Neuropathy_CMT - isolated v0.12 DRP2 Zornitza Stark Marked gene: DRP2 as ready
Hereditary Neuropathy_CMT - isolated v0.12 DRP2 Zornitza Stark Gene: drp2 has been classified as Green List (High Evidence).
Hereditary Neuropathy_CMT - isolated v0.12 DRP2 Zornitza Stark reviewed gene: DRP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 26227883, 11430802, 31217940, 22764250, 29473052; Phenotypes: X-linked Charcot-Marie-Tooth; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Motor Neurone Disease v0.26 PLEKHG5 Bryony Thompson Deleted their review
Motor Neurone Disease v0.26 KIF5A Bryony Thompson Classified gene: KIF5A as Green List (high evidence)
Motor Neurone Disease v0.26 KIF5A Bryony Thompson Gene: kif5a has been classified as Green List (High Evidence).
Motor Neurone Disease v0.25 KIF5A Bryony Thompson gene: KIF5A was added
gene: KIF5A was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: KIF5A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: KIF5A were set to 29342275; 30301576; 29566793
Phenotypes for gene: KIF5A were set to {Amyotrophic lateral sclerosis, susceptibility to, 25} MIM#617921
Review for gene: KIF5A was set to GREEN
Added comment: 12 patients from 9 unrelated families with ALS, had heterozygous LOF variants in the C-terminal region cargo-binding region. Variants causing SPG10 are almost exclusively missense mutations that affect the N-terminal motor domain.
Sources: Expert list
Motor Neurone Disease v0.24 GNE Bryony Thompson gene: GNE was added
gene: GNE was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: GNE was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GNE were set to 29086072
Phenotypes for gene: GNE were set to Amyotrophic lateral sclerosis
Review for gene: GNE was set to RED
Added comment: Single family reported with ALS
Sources: Expert list
Motor Neurone Disease v0.23 GLT8D1 Bryony Thompson Classified gene: GLT8D1 as Green List (high evidence)
Motor Neurone Disease v0.23 GLT8D1 Bryony Thompson Gene: glt8d1 has been classified as Green List (High Evidence).
Motor Neurone Disease v0.22 GLT8D1 Bryony Thompson gene: GLT8D1 was added
gene: GLT8D1 was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: GLT8D1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: GLT8D1 were set to 30811981
Phenotypes for gene: GLT8D1 were set to Amyotrophic lateral sclerosis
Review for gene: GLT8D1 was set to GREEN
Added comment: 14 ALS cases with heterozygous missense (10 cases with p.R92C), and supporting in vitro functional assays and zebrafish model.
Sources: Expert list
Hereditary Neuropathy - complex v0.31 DGUOK Zornitza Stark Marked gene: DGUOK as ready
Hereditary Neuropathy - complex v0.31 DGUOK Zornitza Stark Gene: dguok has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.31 DGUOK Zornitza Stark Classified gene: DGUOK as Green List (high evidence)
Hereditary Neuropathy - complex v0.31 DGUOK Zornitza Stark Gene: dguok has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.30 DGUOK Zornitza Stark gene: DGUOK was added
gene: DGUOK was added to Hereditary Neuropathy - complex. Sources: NHS GMS
Mode of inheritance for gene: DGUOK was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: DGUOK were set to Mitochondrial DNA depletion syndrome 3 (hepatocerebral type), 251880 Portal hypertension, noncirrhotic, 617068 Neonatal liver failure, myopathy, sensory-motor axonal neuropathy
Review for gene: DGUOK was set to GREEN
Added comment: Sources: NHS GMS
Mendeliome v0.1875 DGAT2 Zornitza Stark Marked gene: DGAT2 as ready
Mendeliome v0.1875 DGAT2 Zornitza Stark Gene: dgat2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1875 DGAT2 Zornitza Stark Classified gene: DGAT2 as Amber List (moderate evidence)
Mendeliome v0.1875 DGAT2 Zornitza Stark Gene: dgat2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1874 DGAT2 Zornitza Stark gene: DGAT2 was added
gene: DGAT2 was added to Mendeliome. Sources: Expert Review
Mode of inheritance for gene: DGAT2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: DGAT2 were set to 26786738
Phenotypes for gene: DGAT2 were set to axonal Charcot-Marie-Tooth disease
Review for gene: DGAT2 was set to AMBER
Added comment: Single family (father and son) reported, with supporting in vitro functional assays and a zebrafish model.
Sources: Expert Review
Motor Neurone Disease v0.21 DAO Bryony Thompson gene: DAO was added
gene: DAO was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: DAO was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: DAO were set to 29274788; 29895397; 20368421; 29194436
Phenotypes for gene: DAO were set to Amyotrophic Lateral Sclerosis
Review for gene: DAO was set to RED
Added comment: Many mouse models, but reported variant in a case is R199W, which has gnomAD AF higher than expected for a dominant ALS gene. No compelling evidence in human cases.
Sources: Expert list
Motor Neurone Disease v0.20 EWSR1 Bryony Thompson Classified gene: EWSR1 as Amber List (moderate evidence)
Motor Neurone Disease v0.20 EWSR1 Bryony Thompson Gene: ewsr1 has been classified as Amber List (Moderate Evidence).
Motor Neurone Disease v0.19 EWSR1 Bryony Thompson gene: EWSR1 was added
gene: EWSR1 was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: EWSR1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: EWSR1 were set to 29731676; 22454397
Phenotypes for gene: EWSR1 were set to Amyotrophic lateral sclerosis
Review for gene: EWSR1 was set to AMBER
Added comment: Mouse model and 2 missense reported in 2 ALS cases, but no other reports in ALS cases since 2012
Sources: Expert list
Mendeliome v0.1873 ERLIN1 Bryony Thompson Classified gene: ERLIN1 as Green List (high evidence)
Mendeliome v0.1873 ERLIN1 Bryony Thompson Gene: erlin1 has been classified as Green List (High Evidence).
Mendeliome v0.1872 ERLIN1 Bryony Thompson gene: ERLIN1 was added
gene: ERLIN1 was added to Mendeliome. Sources: Expert list
Mode of inheritance for gene: ERLIN1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ERLIN1 were set to 24482476
Phenotypes for gene: ERLIN1 were set to Spastic paraplegia 62 MIM#615681
Review for gene: ERLIN1 was set to GREEN
Added comment: Three unrelated consanguineous families with early onset pure HSP.
Sources: Expert list
Motor Neurone Disease v0.18 ERLIN1 Bryony Thompson gene: ERLIN1 was added
gene: ERLIN1 was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: ERLIN1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ERLIN1 were set to 29453415
Phenotypes for gene: ERLIN1 were set to Amyotrophic lateral sclerosis
Review for gene: ERLIN1 was set to RED
Added comment: Homozygous varinat segregates with ALS in a single family
Sources: Expert list
Hereditary Neuropathy - complex v0.29 CPOX Zornitza Stark Marked gene: CPOX as ready
Hereditary Neuropathy - complex v0.29 CPOX Zornitza Stark Gene: cpox has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.29 CPOX Zornitza Stark Classified gene: CPOX as Green List (high evidence)
Hereditary Neuropathy - complex v0.29 CPOX Zornitza Stark Gene: cpox has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.28 CPOX Zornitza Stark gene: CPOX was added
gene: CPOX was added to Hereditary Neuropathy - complex. Sources: NHS GMS
Mode of inheritance for gene: CPOX was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: CPOX were set to Coproporphyria, MIM#121300; Harderoporphyria, MIM#121300
Review for gene: CPOX was set to GREEN
Added comment: Acute intermittent porphyria-like phenotype, including neuropathy.
Sources: NHS GMS
Hereditary Neuropathy - complex v0.27 CD59 Zornitza Stark Marked gene: CD59 as ready
Hereditary Neuropathy - complex v0.27 CD59 Zornitza Stark Gene: cd59 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.27 CD59 Zornitza Stark Classified gene: CD59 as Green List (high evidence)
Hereditary Neuropathy - complex v0.27 CD59 Zornitza Stark Gene: cd59 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.26 CD59 Zornitza Stark gene: CD59 was added
gene: CD59 was added to Hereditary Neuropathy - complex. Sources: NHS GMS
Mode of inheritance for gene: CD59 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CD59 were set to 24382084; 23149847
Phenotypes for gene: CD59 were set to Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy 612300
Review for gene: CD59 was set to GREEN
Added comment: Infantile onset of a relapsing-remitting polyneuropathy, often exacerbated by infection, and manifest as hypotonia, limb muscle weakness, and hyporeflexia.
Sources: NHS GMS
Hereditary Neuropathy - complex v0.25 BCKDHB Zornitza Stark Marked gene: BCKDHB as ready
Hereditary Neuropathy - complex v0.25 BCKDHB Zornitza Stark Gene: bckdhb has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.25 BCKDHB Zornitza Stark Classified gene: BCKDHB as Green List (high evidence)
Hereditary Neuropathy - complex v0.25 BCKDHB Zornitza Stark Gene: bckdhb has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.24 BCKDHB Zornitza Stark gene: BCKDHB was added
gene: BCKDHB was added to Hereditary Neuropathy - complex. Sources: NHS GMS
Mode of inheritance for gene: BCKDHB was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: BCKDHB were set to Maple Syrup Urine Disease, Metabolic encephalopathy, elevated branched chain amino acids in urine, acute axonal neuropathy
Review for gene: BCKDHB was set to GREEN
Added comment: Sources: NHS GMS
Hereditary Neuropathy_CMT - isolated v0.12 ATL3 Zornitza Stark Marked gene: ATL3 as ready
Hereditary Neuropathy_CMT - isolated v0.12 ATL3 Zornitza Stark Gene: atl3 has been classified as Green List (High Evidence).
Hereditary Neuropathy_CMT - isolated v0.12 ATL3 Zornitza Stark Publications for gene: ATL3 were set to 24459106; 30666337; 30339187; 24736309
Hereditary Neuropathy_CMT - isolated v0.11 ATL3 Zornitza Stark Publications for gene: ATL3 were set to
Hereditary Neuropathy_CMT - isolated v0.10 ATL3 Zornitza Stark reviewed gene: ATL3: Rating: GREEN; Mode of pathogenicity: None; Publications: 24459106, 30666337, 30339187, 24736309; Phenotypes: Neuropathy, hereditary sensory, type IF, MIM# 615632; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Motor Neurone Disease v0.17 ERBB4 Bryony Thompson Marked gene: ERBB4 as ready
Motor Neurone Disease v0.17 ERBB4 Bryony Thompson Gene: erbb4 has been classified as Green List (High Evidence).
Motor Neurone Disease v0.17 ERBB4 Bryony Thompson Classified gene: ERBB4 as Green List (high evidence)
Motor Neurone Disease v0.17 ERBB4 Bryony Thompson Gene: erbb4 has been classified as Green List (High Evidence).
Motor Neurone Disease v0.16 ERBB4 Bryony Thompson gene: ERBB4 was added
gene: ERBB4 was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: ERBB4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: ERBB4 were set to 24119685; 28889094
Phenotypes for gene: ERBB4 were set to Amyotrophic lateral sclerosis 19 MIM#615515
Review for gene: ERBB4 was set to GREEN
Added comment: At least 4 cases with ALS
Sources: Expert list
Hereditary Neuropathy_CMT - isolated v0.10 ARHGEF10 Zornitza Stark Classified gene: ARHGEF10 as Green List (high evidence)
Hereditary Neuropathy_CMT - isolated v0.10 ARHGEF10 Zornitza Stark Gene: arhgef10 has been classified as Green List (High Evidence).
Hereditary Neuropathy_CMT - isolated v0.9 ARHGEF10 Zornitza Stark changed review comment from: Single family reported in 2003 with slowed nerve conduction velocities but no other clinical findings. Another individual reported in a large cohort.; to: Single family reported in 2003 with slowed nerve conduction velocities but no other clinical findings. Two others in CMT cohorts, plus functional data.
Hereditary Neuropathy_CMT - isolated v0.9 ARHGEF10 Zornitza Stark edited their review of gene: ARHGEF10: Changed rating: GREEN
Hereditary Neuropathy_CMT - isolated v0.9 ARHGEF10 Zornitza Stark Marked gene: ARHGEF10 as ready
Hereditary Neuropathy_CMT - isolated v0.9 ARHGEF10 Zornitza Stark Gene: arhgef10 has been classified as Amber List (Moderate Evidence).
Hereditary Neuropathy_CMT - isolated v0.9 ARHGEF10 Zornitza Stark Classified gene: ARHGEF10 as Amber List (moderate evidence)
Hereditary Neuropathy_CMT - isolated v0.9 ARHGEF10 Zornitza Stark Gene: arhgef10 has been classified as Amber List (Moderate Evidence).
Hereditary Neuropathy_CMT - isolated v0.8 ARHGEF10 Zornitza Stark reviewed gene: ARHGEF10: Rating: AMBER; Mode of pathogenicity: None; Publications: 14508709, 25025039; Phenotypes: Slowed nerve conduction velocity, MIM# 608236; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary Neuropathy - complex v0.23 APOA1 Zornitza Stark Marked gene: APOA1 as ready
Hereditary Neuropathy - complex v0.23 APOA1 Zornitza Stark Gene: apoa1 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.23 APOA1 Zornitza Stark Classified gene: APOA1 as Green List (high evidence)
Hereditary Neuropathy - complex v0.23 APOA1 Zornitza Stark Gene: apoa1 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.22 APOA1 Zornitza Stark gene: APOA1 was added
gene: APOA1 was added to Hereditary Neuropathy - complex. Sources: NHS GMS
Mode of inheritance for gene: APOA1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: APOA1 were set to Amyloidosis, 3 or more types 105200; Renal failure, Axonal sensory-motor neuropathy, amyloid nephropathy
Review for gene: APOA1 was set to GREEN
Added comment: Neuropathy is a predominant feature, particularly of the Iowa type, associated with p.Gly26Arg
Sources: NHS GMS
Mendeliome v0.1871 BTBD7 Zornitza Stark Marked gene: BTBD7 as ready
Mendeliome v0.1871 BTBD7 Zornitza Stark Added comment: Comment when marking as ready: Agreed, no evidence currently for Mendelian gene-disease association.
Mendeliome v0.1871 BTBD7 Zornitza Stark Gene: btbd7 has been classified as Red List (Low Evidence).
Mendeliome v0.1871 BTBD7 Zornitza Stark Classified gene: BTBD7 as Red List (low evidence)
Mendeliome v0.1871 BTBD7 Zornitza Stark Gene: btbd7 has been classified as Red List (Low Evidence).
Mendeliome v0.1870 NOS1AP Zornitza Stark Marked gene: NOS1AP as ready
Mendeliome v0.1870 NOS1AP Zornitza Stark Added comment: Comment when marking as ready: Agreed, cannot find evidence for Mendelian gene-disease association.
Mendeliome v0.1870 NOS1AP Zornitza Stark Gene: nos1ap has been classified as Red List (Low Evidence).
Mendeliome v0.1870 NOS1AP Zornitza Stark Classified gene: NOS1AP as Red List (low evidence)
Mendeliome v0.1870 NOS1AP Zornitza Stark Gene: nos1ap has been classified as Red List (Low Evidence).
Mendeliome v0.1869 ARID2 Zornitza Stark Marked gene: ARID2 as ready
Mendeliome v0.1869 ARID2 Zornitza Stark Gene: arid2 has been classified as Green List (High Evidence).
Mendeliome v0.1869 ARID2 Zornitza Stark Phenotypes for gene: ARID2 were changed from to Coffin-Siris syndrome 6, MIM#617808
Mendeliome v0.1868 ARID2 Zornitza Stark Publications for gene: ARID2 were set to 30838730
Mendeliome v0.1867 ARID2 Zornitza Stark Publications for gene: ARID2 were set to
Mendeliome v0.1866 ARID2 Zornitza Stark Mode of inheritance for gene: ARID2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1865 DYNC1H1 Zornitza Stark Marked gene: DYNC1H1 as ready
Mendeliome v0.1865 DYNC1H1 Zornitza Stark Gene: dync1h1 has been classified as Green List (High Evidence).
Mendeliome v0.1865 DYNC1H1 Zornitza Stark Phenotypes for gene: DYNC1H1 were changed from to Charcot-Marie-Tooth disease, axonal, type 20; Mental retardation, autosomal dominant 13; Spinal muscular atrophy, lower extremity-predominant 1
Mendeliome v0.1864 DYNC1H1 Zornitza Stark Publications for gene: DYNC1H1 were set to
Mendeliome v0.1863 DYNC1H1 Zornitza Stark Mode of pathogenicity for gene: DYNC1H1 was changed from to Other
Mendeliome v0.1862 DYNC1H1 Zornitza Stark Mode of inheritance for gene: DYNC1H1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2498 PQBP1 Zornitza Stark Marked gene: PQBP1 as ready
Intellectual disability syndromic and non-syndromic v0.2498 PQBP1 Zornitza Stark Gene: pqbp1 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2498 PQBP1 Zornitza Stark Phenotypes for gene: PQBP1 were changed from to Renpenning syndrome, MIM#309500
Intellectual disability syndromic and non-syndromic v0.2497 PQBP1 Zornitza Stark Publications for gene: PQBP1 were set to
Intellectual disability syndromic and non-syndromic v0.2496 PQBP1 Zornitza Stark Mode of inheritance for gene: PQBP1 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Intellectual disability syndromic and non-syndromic v0.2495 PQBP1 Zornitza Stark reviewed gene: PQBP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 31840929, 14634649, 20410308; Phenotypes: Renpenning syndrome, MIM#309500; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Mendeliome v0.1861 PQBP1 Zornitza Stark Marked gene: PQBP1 as ready
Mendeliome v0.1861 PQBP1 Zornitza Stark Gene: pqbp1 has been classified as Green List (High Evidence).
Mendeliome v0.1861 PQBP1 Zornitza Stark Phenotypes for gene: PQBP1 were changed from to Renpenning syndrome, MIM#309500
Mendeliome v0.1860 PQBP1 Zornitza Stark Publications for gene: PQBP1 were set to
Mendeliome v0.1859 PQBP1 Zornitza Stark Mode of pathogenicity for gene: PQBP1 was changed from to Other
Mendeliome v0.1858 PQBP1 Zornitza Stark Mode of inheritance for gene: PQBP1 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Mendeliome v0.1857 CHD3 Zornitza Stark Marked gene: CHD3 as ready
Mendeliome v0.1857 CHD3 Zornitza Stark Added comment: Comment when marking as ready: Over 30 unrelated individuals reported.
Mendeliome v0.1857 CHD3 Zornitza Stark Gene: chd3 has been classified as Green List (High Evidence).
Mendeliome v0.1857 CHD3 Zornitza Stark Phenotypes for gene: CHD3 were changed from to Snijders Blok-Campeau syndrome (618205)
Mendeliome v0.1856 CHD3 Zornitza Stark Publications for gene: CHD3 were set to
Mendeliome v0.1855 CHD3 Zornitza Stark Mode of pathogenicity for gene: CHD3 was changed from to Other
Mendeliome v0.1854 CHD3 Zornitza Stark Mode of inheritance for gene: CHD3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Dilated Cardiomyopathy v0.25 TTN Zornitza Stark reviewed gene: TTN: Rating: GREEN; Mode of pathogenicity: None; Publications: 22335739; Phenotypes: Cardiomyopathy, dilated, 1G, MIM#604145; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Dilated Cardiomyopathy v0.25 TTN Zornitza Stark Marked gene: TTN as ready
Dilated Cardiomyopathy v0.25 TTN Zornitza Stark Gene: ttn has been classified as Green List (High Evidence).
Dilated Cardiomyopathy v0.25 TTN Zornitza Stark Publications for gene: TTN were set to
Dilated Cardiomyopathy v0.24 TTN Zornitza Stark Phenotypes for gene: TTN were changed from to Cardiomyopathy, dilated, 1G, MIM#604145
Dilated Cardiomyopathy v0.23 TTN Zornitza Stark Mode of inheritance for gene: TTN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Arthrogryposis v0.35 MYH7 Zornitza Stark Marked gene: MYH7 as ready
Arthrogryposis v0.35 MYH7 Zornitza Stark Gene: myh7 has been classified as Red List (Low Evidence).
Arthrogryposis v0.35 MYH7 Zornitza Stark Phenotypes for gene: MYH7 were changed from to Laing distal myopathy 160500; Myopathy, myosin storage, autosomal dominant 608358; Myopathy, myosin storage, autosomal recessive 255160; Scapuloperoneal syndrome, myopathic type 181430
Arthrogryposis v0.34 MYH7 Zornitza Stark Mode of inheritance for gene: MYH7 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Arthrogryposis v0.33 MYH7 Zornitza Stark Publications for gene: MYH7 were set to
Arthrogryposis v0.32 MYH7 Zornitza Stark Classified gene: MYH7 as Red List (low evidence)
Arthrogryposis v0.32 MYH7 Zornitza Stark Gene: myh7 has been classified as Red List (Low Evidence).
Arthrogryposis v0.31 MYH7 Zornitza Stark reviewed gene: MYH7: Rating: RED; Mode of pathogenicity: None; Publications: 27519903; Phenotypes: Laing distal myopathy, MIM# 160500; Mode of inheritance: None
Intellectual disability syndromic and non-syndromic v0.2495 DLG3 Zornitza Stark Marked gene: DLG3 as ready
Intellectual disability syndromic and non-syndromic v0.2495 DLG3 Zornitza Stark Gene: dlg3 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2495 DLG3 Zornitza Stark Phenotypes for gene: DLG3 were changed from to Mental retardation, X-linked 90, MIM#300850
Intellectual disability syndromic and non-syndromic v0.2494 DLG3 Zornitza Stark Publications for gene: DLG3 were set to
Intellectual disability syndromic and non-syndromic v0.2493 DLG3 Zornitza Stark Mode of inheritance for gene: DLG3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Intellectual disability syndromic and non-syndromic v0.2492 DLG3 Zornitza Stark reviewed gene: DLG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 28777483, 24721225; Phenotypes: Mental retardation, X-linked 90, MIM#300850; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Mendeliome v0.1853 DLG3 Zornitza Stark Marked gene: DLG3 as ready
Mendeliome v0.1853 DLG3 Zornitza Stark Gene: dlg3 has been classified as Green List (High Evidence).
Mendeliome v0.1853 DLG3 Zornitza Stark Phenotypes for gene: DLG3 were changed from to Mental retardation, X-linked 90, MIM#300850
Mendeliome v0.1852 DLG3 Zornitza Stark Publications for gene: DLG3 were set to
Mendeliome v0.1851 DLG3 Zornitza Stark Mode of inheritance for gene: DLG3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Hypertrophic cardiomyopathy_HCM v0.18 CALR3 Kristin Rigbye reviewed gene: CALR3: Rating: RED; Mode of pathogenicity: Other; Publications: 29988065; Phenotypes: Hypertrophic cardiomyopathy; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Bleeding and Platelet Disorders v0.16 FBN2 Zornitza Stark Marked gene: FBN2 as ready
Bleeding and Platelet Disorders v0.16 FBN2 Zornitza Stark Gene: fbn2 has been classified as Red List (Low Evidence).
Bleeding and Platelet Disorders v0.16 FBN2 Zornitza Stark Phenotypes for gene: FBN2 were changed from to Contractural arachnodactyly, congenital 121050; Macular degeneration, early-onset 616118
Bleeding and Platelet Disorders v0.15 FBN2 Zornitza Stark Mode of inheritance for gene: FBN2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Bleeding and Platelet Disorders v0.14 FBN2 Zornitza Stark Classified gene: FBN2 as Red List (low evidence)
Bleeding and Platelet Disorders v0.14 FBN2 Zornitza Stark Gene: fbn2 has been classified as Red List (Low Evidence).
Bleeding and Platelet Disorders v0.13 FBN2 Zornitza Stark reviewed gene: FBN2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Contractural arachnodactyly, congenital 121050, Macular degeneration, early-onset 616118; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Arthrogryposis v0.31 FBN2 Zornitza Stark Marked gene: FBN2 as ready
Arthrogryposis v0.31 FBN2 Zornitza Stark Gene: fbn2 has been classified as Green List (High Evidence).
Arthrogryposis v0.31 FBN2 Zornitza Stark Phenotypes for gene: FBN2 were changed from to Contractural arachnodactyly, congenital, MIM# 121050
Arthrogryposis v0.30 FBN2 Zornitza Stark Mode of inheritance for gene: FBN2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Arthrogryposis v0.29 FBN2 Zornitza Stark reviewed gene: FBN2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Contractural arachnodactyly, congenital, MIM# 121050; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Aortopathy_Connective Tissue Disorders v0.13 FBN2 Zornitza Stark Marked gene: FBN2 as ready
Aortopathy_Connective Tissue Disorders v0.13 FBN2 Zornitza Stark Gene: fbn2 has been classified as Green List (High Evidence).
Aortopathy_Connective Tissue Disorders v0.13 FBN2 Zornitza Stark Phenotypes for gene: FBN2 were changed from to Contractural arachnodactyly, congenital, MIM# 121050
Aortopathy_Connective Tissue Disorders v0.12 FBN2 Zornitza Stark Mode of inheritance for gene: FBN2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Aortopathy_Connective Tissue Disorders v0.11 FBN2 Zornitza Stark edited their review of gene: FBN2: Changed phenotypes: Contractural arachnodactyly, congenital, MIM# 121050
Aortopathy_Connective Tissue Disorders v0.11 FBN2 Zornitza Stark reviewed gene: FBN2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Macular degeneration, early-onset, MIM# 616118; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1850 FBN2 Zornitza Stark Marked gene: FBN2 as ready
Mendeliome v0.1850 FBN2 Zornitza Stark Added comment: Comment when marking as ready: The gene-disease association with Contractual arachnodactyly is extremely well established. The gene-disease association with macular degeneration much less so. There are ~4 families reported in the literature, and some discussion about whether the contribution of rare FBN2 variants in this context are under a 'monogenic' or 'polygenic' model.
Mendeliome v0.1850 FBN2 Zornitza Stark Gene: fbn2 has been classified as Green List (High Evidence).
Mendeliome v0.1850 FBN2 Zornitza Stark Publications for gene: FBN2 were set to 19473076; 11068201
Mendeliome v0.1849 FBN2 Zornitza Stark Phenotypes for gene: FBN2 were changed from to Contractural arachnodactyly, congenital 121050; Macular degeneration, early-onset 616118
Mendeliome v0.1848 FBN2 Zornitza Stark Publications for gene: FBN2 were set to
Mendeliome v0.1847 FBN2 Zornitza Stark Mode of inheritance for gene: FBN2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1846 BTBD7 Elena Savva reviewed gene: BTBD7: Rating: RED; Mode of pathogenicity: Other; Publications: ; Phenotypes: ; Mode of inheritance: Unknown
Hereditary Neuropathy - complex v0.21 AIFM1 Zornitza Stark Marked gene: AIFM1 as ready
Hereditary Neuropathy - complex v0.21 AIFM1 Zornitza Stark Gene: aifm1 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.21 AIFM1 Zornitza Stark Publications for gene: AIFM1 were set to
Hereditary Neuropathy - complex v0.20 AIFM1 Zornitza Stark reviewed gene: AIFM1: Rating: GREEN; Mode of pathogenicity: None; Publications: 3856385, 22019070, 26173962, 25583628; Phenotypes: Combined oxidative phosphorylation deficiency 6, Cowchock syndrome; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Hereditary Neuropathy - complex v0.20 AGXT Zornitza Stark Marked gene: AGXT as ready
Hereditary Neuropathy - complex v0.20 AGXT Zornitza Stark Gene: agxt has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.20 AGXT Zornitza Stark Classified gene: AGXT as Green List (high evidence)
Hereditary Neuropathy - complex v0.20 AGXT Zornitza Stark Gene: agxt has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.19 AGXT Zornitza Stark gene: AGXT was added
gene: AGXT was added to Hereditary Neuropathy - complex. Sources: NHS GMS
Mode of inheritance for gene: AGXT was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: AGXT were set to Hyperoxaluria, primary, type 1, MIM#259900
Review for gene: AGXT was set to GREEN
Added comment: Multi-system oxalate deposition including leading to neuropathy.
Sources: NHS GMS
Dystonia_Superpanel v0.0 Bryony Thompson Added Panel Dystonia Superpanel
Set child panels to: Dystonia - complex_RMH; Dystonia - isolated/combined_RMH
Set panel types to: Royal Melbourne Hospital
Mendeliome v0.1846 AGTPBP1 Zornitza Stark Marked gene: AGTPBP1 as ready
Mendeliome v0.1846 AGTPBP1 Zornitza Stark Gene: agtpbp1 has been classified as Green List (High Evidence).
Mendeliome v0.1846 AGTPBP1 Zornitza Stark Classified gene: AGTPBP1 as Green List (high evidence)
Mendeliome v0.1846 AGTPBP1 Zornitza Stark Gene: agtpbp1 has been classified as Green List (High Evidence).
Mendeliome v0.1845 AGTPBP1 Zornitza Stark gene: AGTPBP1 was added
gene: AGTPBP1 was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: AGTPBP1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: AGTPBP1 were set to 30420557
Phenotypes for gene: AGTPBP1 were set to Early onset cerebellar atrophy, developmental delay, and feeding and respiratory difficulties, severe motor neuronopathy; Neurodegeneration, childhood-onset, with cerebellar atrophy, 618276
Review for gene: AGTPBP1 was set to GREEN
Added comment: Thirteen individuals with bi-allelic variants in this gene, complex neurological phenotype of dev delay/ID, cerebellar atrophy and neuropathy, severe progressive course in six.
Sources: NHS GMS
Intellectual disability syndromic and non-syndromic v0.2492 AGTPBP1 Zornitza Stark Marked gene: AGTPBP1 as ready
Intellectual disability syndromic and non-syndromic v0.2492 AGTPBP1 Zornitza Stark Gene: agtpbp1 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2492 AGTPBP1 Zornitza Stark Classified gene: AGTPBP1 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2492 AGTPBP1 Zornitza Stark Gene: agtpbp1 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2491 AGTPBP1 Zornitza Stark gene: AGTPBP1 was added
gene: AGTPBP1 was added to Intellectual disability syndromic and non-syndromic. Sources: NHS GMS
Mode of inheritance for gene: AGTPBP1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: AGTPBP1 were set to 30420557
Phenotypes for gene: AGTPBP1 were set to Early onset cerebellar atrophy, developmental delay, and feeding and respiratory difficulties, severe motor neuronopathy; Neurodegeneration, childhood-onset, with cerebellar atrophy, 618276
Review for gene: AGTPBP1 was set to GREEN
Added comment: Thirteen individuals reported, clinical presentation was with developmental delay, though six went on to have a progressive neurological course. Other features include cerebellar atrophy and neuropathy.
Sources: NHS GMS
Regression v0.101 AGTPBP1 Zornitza Stark Marked gene: AGTPBP1 as ready
Regression v0.101 AGTPBP1 Zornitza Stark Gene: agtpbp1 has been classified as Green List (High Evidence).
Regression v0.101 AGTPBP1 Zornitza Stark Classified gene: AGTPBP1 as Green List (high evidence)
Regression v0.101 AGTPBP1 Zornitza Stark Gene: agtpbp1 has been classified as Green List (High Evidence).
Regression v0.100 AGTPBP1 Zornitza Stark gene: AGTPBP1 was added
gene: AGTPBP1 was added to Regression. Sources: NHS GMS
Mode of inheritance for gene: AGTPBP1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: AGTPBP1 were set to 30420557
Phenotypes for gene: AGTPBP1 were set to Early onset cerebellar atrophy, developmental delay, and feeding and respiratory difficulties, severe motor neuronopathy; Neurodegeneration, childhood-onset, with cerebellar atrophy, 618276
Review for gene: AGTPBP1 was set to GREEN
Added comment: Thirteen individuals with bi-allelic variants in this gene, six of those had a progressive course.
Sources: NHS GMS
Hereditary Neuropathy - complex v0.18 AGTPBP1 Zornitza Stark Marked gene: AGTPBP1 as ready
Hereditary Neuropathy - complex v0.18 AGTPBP1 Zornitza Stark Gene: agtpbp1 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.18 AGTPBP1 Zornitza Stark Classified gene: AGTPBP1 as Green List (high evidence)
Hereditary Neuropathy - complex v0.18 AGTPBP1 Zornitza Stark Gene: agtpbp1 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.17 AGTPBP1 Zornitza Stark gene: AGTPBP1 was added
gene: AGTPBP1 was added to Hereditary Neuropathy - complex. Sources: NHS GMS
Mode of inheritance for gene: AGTPBP1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: AGTPBP1 were set to 30420557
Phenotypes for gene: AGTPBP1 were set to Early onset cerebellar atrophy, developmental delay, and feeding and respiratory difficulties, severe motor neuronopathy; Neurodegeneration, childhood-onset, with cerebellar atrophy, 618276
Review for gene: AGTPBP1 was set to GREEN
Added comment: Thirteen individuals with bi-allelic variants in this gene, neuropathy is a major feature.
Sources: NHS GMS
Hereditary Neuropathy - complex v0.16 AAAS Zornitza Stark Marked gene: AAAS as ready
Hereditary Neuropathy - complex v0.16 AAAS Zornitza Stark Gene: aaas has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.16 AAAS Zornitza Stark Phenotypes for gene: AAAS were changed from HMSN; Glucocorticoid deficiency with achalasia to HMSN; Glucocorticoid deficiency with achalasia; Achalasia-addisonianism-alacrimia syndrome, MIM# 231550
Hereditary Neuropathy - complex v0.15 AAAS Zornitza Stark reviewed gene: AAAS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Achalasia-addisonianism-alacrimia syndrome, MIM# 231550; Mode of inheritance: None
Intellectual disability syndromic and non-syndromic v0.2490 ADGRG6 Zornitza Stark reviewed gene: ADGRG6: Rating: RED; Mode of pathogenicity: None; Publications: 30549416, 26004201; Phenotypes: Lethal congenital contracture syndrome 9, OMIM #616503; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1844 ADGRG6 Zornitza Stark Publications for gene: ADGRG6 were set to 30549416
Mendeliome v0.1843 ADGRG6 Zornitza Stark Classified gene: ADGRG6 as Green List (high evidence)
Mendeliome v0.1843 ADGRG6 Zornitza Stark Gene: adgrg6 has been classified as Green List (High Evidence).
Mendeliome v0.1842 ADGRG6 Zornitza Stark edited their review of gene: ADGRG6: Added comment: Three families reported originally with severe prenatal-onset arthrogryposis (PMID: 26004201), one family with more complex neurological phenotype (PMID:30549416).; Changed rating: GREEN; Changed publications: 30549416, 26004201; Changed phenotypes: Lethal congenital contracture syndrome 9, OMIM #616503; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Arthrogryposis v0.29 ADGRG6 Zornitza Stark Marked gene: ADGRG6 as ready
Arthrogryposis v0.29 ADGRG6 Zornitza Stark Added comment: Comment when marking as ready: Gene previously known as GPR126.
Arthrogryposis v0.29 ADGRG6 Zornitza Stark Gene: adgrg6 has been classified as Green List (High Evidence).
Arthrogryposis v0.29 ADGRG6 Zornitza Stark Classified gene: ADGRG6 as Green List (high evidence)
Arthrogryposis v0.29 ADGRG6 Zornitza Stark Gene: adgrg6 has been classified as Green List (High Evidence).
Arthrogryposis v0.28 ADGRG6 Zornitza Stark Publications for gene: ADGRG6 were set to 30549416; 26004201
Arthrogryposis v0.27 ADGRG6 Zornitza Stark Publications for gene: ADGRG6 were set to 30549416
Arthrogryposis v0.26 ADGRG6 Zornitza Stark Classified gene: ADGRG6 as Green List (high evidence)
Arthrogryposis v0.26 ADGRG6 Zornitza Stark Gene: adgrg6 has been classified as Green List (High Evidence).
Mendeliome v0.1842 NOS1AP Crystle Lee reviewed gene: NOS1AP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Mendeliome v0.1842 ARID2 Elena Savva reviewed gene: ARID2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID:30838730; Phenotypes: Coffin-Siris syndrome 6; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Current diagnostic: yes
Mendeliome v0.1842 DYNC1H1 Elena Savva reviewed gene: DYNC1H1: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID: 25512093, 28196890; Phenotypes: Charcot-Marie-Tooth disease, axonal, type 20, Mental retardation, autosomal dominant 13, Spinal muscular atrophy, lower extremity-predominant 1; Mode of inheritance: None
Mendeliome v0.1842 PQBP1 Elena Savva reviewed gene: PQBP1: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID:31840929, 14634649, 20410308; Phenotypes: Renpenning syndrome; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males); Current diagnostic: yes
Mendeliome v0.1842 CHD3 Elena Savva reviewed gene: CHD3: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID:30397230; Phenotypes: Snijders Blok-Campeau syndrome (618205); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Dilated Cardiomyopathy v0.22 TTN Elena Savva reviewed gene: TTN: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 25589632, 28045975; Phenotypes: Cardiomyopathy, dilated, 1G, 604145, Cardiomyopathy, familial hypertrophic, 9, 613765, Muscular dystrophy, limb-girdle, autosomal recessive 10, 608807, (LGMDR10), Myopathy, myofibrillar, 9, with early respiratory failure, 603689, Salih myopathy, 611705, Tibial muscular dystrophy, tardive, 600334; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Arthrogryposis v0.25 MYH7 Elena Savva reviewed gene: MYH7: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID 29300372, 30924982, 24714796, 30623132; Phenotypes: Cardiomyopathy, dilated, 1S 613426, Cardiomyopathy, hypertrophic, 1 192600, Laing distal myopathy 160500, Left ventricular noncompaction 5 613426, Myopathy, myosin storage, autosomal dominant 608358, Myopathy, myosin storage, autosomal recessive 255160, Scapuloperoneal syndrome, myopathic type 181430; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mendeliome v0.1842 DLG3 Elena Savva reviewed gene: DLG3: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID 28777483; Phenotypes: Mental retardation, X-linked 90; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Mendeliome v0.1842 FBN2 Elena Savva reviewed gene: FBN2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID 19473076, 11068201; Phenotypes: Contractural arachnodactyly, congenital 121050, Macular degeneration, early-onset 616118; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Current diagnostic: yes
Arthrogryposis v0.25 ADGRG6 Crystle Lee reviewed gene: ADGRG6: Rating: GREEN; Mode of pathogenicity: None; Publications: 26004201; Phenotypes: Lethal congenital contracture syndrome 9 (MIM#616503); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Motor Neurone Disease v0.15 LAS1L Bryony Thompson Deleted their review
Motor Neurone Disease v0.15 IGHMBP2 Bryony Thompson Deleted their review
Motor Neurone Disease v0.15 EXOSC8 Bryony Thompson Deleted their review
Motor Neurone Disease v0.15 DCTN1 Bryony Thompson Deleted their review
Incidentalome v0.16 CCNF Bryony Thompson Classified gene: CCNF as Green List (high evidence)
Incidentalome v0.16 CCNF Bryony Thompson Gene: ccnf has been classified as Green List (High Evidence).
Incidentalome v0.15 CCNF Bryony Thompson gene: CCNF was added
gene: CCNF was added to Incidentalome. Sources: Expert list
Mode of inheritance for gene: CCNF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CCNF were set to 27080313; 31577344
Phenotypes for gene: CCNF were set to amyotrophic lateral sclerosis with/without frontotemporal dementia
Review for gene: CCNF was set to GREEN
Added comment: >3 families/cases and supporting functional evidence
Sources: Expert list
Early-onset Dementia v0.44 CCNF Bryony Thompson Marked gene: CCNF as ready
Early-onset Dementia v0.44 CCNF Bryony Thompson Gene: ccnf has been classified as Green List (High Evidence).
Early-onset Dementia v0.44 CCNF Bryony Thompson Classified gene: CCNF as Green List (high evidence)
Early-onset Dementia v0.44 CCNF Bryony Thompson Gene: ccnf has been classified as Green List (High Evidence).
Early-onset Dementia v0.43 CCNF Bryony Thompson gene: CCNF was added
gene: CCNF was added to Early-onset Dementia. Sources: Expert list
Mode of inheritance for gene: CCNF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CCNF were set to 27080313
Phenotypes for gene: CCNF were set to amyotrophic lateral sclerosis with/without frontotemporal dementia
Review for gene: CCNF was set to GREEN
Added comment: Four cases, within three families with FTD with/without ALS.
Sources: Expert list
Motor Neurone Disease v0.15 CCNF Bryony Thompson Marked gene: CCNF as ready
Motor Neurone Disease v0.15 CCNF Bryony Thompson Gene: ccnf has been classified as Green List (High Evidence).
Motor Neurone Disease v0.15 CCNF Bryony Thompson Classified gene: CCNF as Green List (high evidence)
Motor Neurone Disease v0.15 CCNF Bryony Thompson Gene: ccnf has been classified as Green List (High Evidence).
Motor Neurone Disease v0.14 CCNF Bryony Thompson gene: CCNF was added
gene: CCNF was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: CCNF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CCNF were set to 29102476; 31577344; 27080313; 28105640; 31445393; 28852778
Phenotypes for gene: CCNF were set to amyotrophic lateral sclerosis with/without frontotemporal dementia
Review for gene: CCNF was set to GREEN
Added comment: >3 cases/families and supporting functional evidence
Sources: Expert list
Incidentalome v0.14 ANXA11 Bryony Thompson Classified gene: ANXA11 as Green List (high evidence)
Incidentalome v0.14 ANXA11 Bryony Thompson Gene: anxa11 has been classified as Green List (High Evidence).
Motor Neurone Disease v0.13 ASCC1 Bryony Thompson Deleted their review
Incidentalome v0.13 ANXA11 Bryony Thompson gene: ANXA11 was added
gene: ANXA11 was added to Incidentalome. Sources: Expert list
Mode of inheritance for gene: ANXA11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: ANXA11 were set to 28469040; 29845112; 30109997
Phenotypes for gene: ANXA11 were set to Amytrophic lateral sclerosis 23 MIM#617839
Review for gene: ANXA11 was set to GREEN
Added comment: 4 different missense variants in 10 patients from 7 unrelated families with amyotrophic lateral sclerosis and functional assays supporting association.
Sources: Expert list
Motor Neurone Disease v0.13 ANXA11 Bryony Thompson Classified gene: ANXA11 as Green List (high evidence)
Motor Neurone Disease v0.13 ANXA11 Bryony Thompson Gene: anxa11 has been classified as Green List (High Evidence).
Early-onset Parkinson disease v0.27 Bryony Thompson Panel name changed from Early onset Parkinson disease to Early-onset Parkinson disease
Panel types changed to Melbourne Genomics; Victorian Clinical Genetics Services; Royal Melbourne Hospital
Early-onset Parkinson disease v0.26 VPS13C Bryony Thompson Marked gene: VPS13C as ready
Early-onset Parkinson disease v0.26 VPS13C Bryony Thompson Gene: vps13c has been classified as Green List (High Evidence).
Early-onset Parkinson disease v0.26 VPS13C Bryony Thompson Classified gene: VPS13C as Green List (high evidence)
Early-onset Parkinson disease v0.26 VPS13C Bryony Thompson Gene: vps13c has been classified as Green List (High Evidence).
Early-onset Parkinson disease v0.25 VPS13C Bryony Thompson gene: VPS13C was added
gene: VPS13C was added to Early onset Parkinson disease. Sources: Expert list
Mode of inheritance for gene: VPS13C was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: VPS13C were set to 26942284; 30452786; 28862745
Phenotypes for gene: VPS13C were set to Parkinson disease 23, autosomal recessive, early onset MIM#616840
Review for gene: VPS13C was set to GREEN
Added comment: >3 cases with biallelic variants.
Sources: Expert list
Early-onset Parkinson disease v0.24 TWNK Bryony Thompson Mode of inheritance for gene: TWNK was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early-onset Parkinson disease v0.23 TWNK Bryony Thompson Marked gene: TWNK as ready
Early-onset Parkinson disease v0.23 TWNK Bryony Thompson Gene: twnk has been classified as Green List (High Evidence).
Early-onset Parkinson disease v0.23 TWNK Bryony Thompson reviewed gene: TWNK: Rating: GREEN; Mode of pathogenicity: None; Publications: 24076137, 22949510, 22580846, 19353676; Phenotypes: Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3 MIM#609286; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Lymphoedema_syndromic v0.1 CHD7 Zornitza Stark Marked gene: CHD7 as ready
Lymphoedema_syndromic v0.1 CHD7 Zornitza Stark Gene: chd7 has been classified as Red List (Low Evidence).
Lymphoedema_syndromic v0.1 CHD7 Zornitza Stark Classified gene: CHD7 as Red List (low evidence)
Lymphoedema_syndromic v0.1 CHD7 Zornitza Stark Gene: chd7 has been classified as Red List (Low Evidence).
Lymphoedema_syndromic v0.0 CHD7 Zornitza Stark reviewed gene: CHD7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: CHARGE syndrome, MIM# 214800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2490 NAA15 Ee Ming Wong reviewed gene: NAA15: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 31127942; Phenotypes: Mental retardation, autosomal dominant 50, 617787 (3), NAA15-related syndrome (PMID: 31127942); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Intellectual disability syndromic and non-syndromic v0.2490 NR2F2 Sue White Classified gene: NR2F2 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2490 NR2F2 Sue White Gene: nr2f2 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2489 NR2F2 Sue White gene: NR2F2 was added
gene: NR2F2 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature
Mode of inheritance for gene: NR2F2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: NR2F2 were set to 29478779; 29663647
Phenotypes for gene: NR2F2 were set to mild intellectual disability; congenital heart disease; disorder of sexual differentiation; dysmorphic features
Penetrance for gene: NR2F2 were set to Complete
Review for gene: NR2F2 was set to AMBER
Added comment: Established gene for congenital heart disease and DSD and emerging gene for ID. 2 unrelated individuals published with mild or borderline ID, dysmorphism and de novo truncating/missense variants.
Sources: Literature
Regression v0.99 EIF2AK2 Zornitza Stark Marked gene: EIF2AK2 as ready
Regression v0.99 EIF2AK2 Zornitza Stark Gene: eif2ak2 has been classified as Green List (High Evidence).
Regression v0.99 EIF2AK2 Zornitza Stark Classified gene: EIF2AK2 as Green List (high evidence)
Regression v0.99 EIF2AK2 Zornitza Stark Gene: eif2ak2 has been classified as Green List (High Evidence).
Regression v0.98 EIF2AK2 Zornitza Stark gene: EIF2AK2 was added
gene: EIF2AK2 was added to Regression. Sources: Literature
Mode of inheritance for gene: EIF2AK2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: EIF2AK2 were set to 32197074
Phenotypes for gene: EIF2AK2 were set to Intellectual disability; white matter abnormalities; ataxia; regression with febrile illness
Review for gene: EIF2AK2 was set to GREEN
Added comment: Eight individuals with de novo variants and complex neurodevelopmental phenotype.
Sources: Literature
Regression v0.97 Zornitza Stark Panel types changed to Victorian Clinical Genetics Services; Rare Disease
Mendeliome v0.1842 EIF2AK2 Zornitza Stark Marked gene: EIF2AK2 as ready
Mendeliome v0.1842 EIF2AK2 Zornitza Stark Gene: eif2ak2 has been classified as Green List (High Evidence).
Mendeliome v0.1842 EIF2AK2 Zornitza Stark Classified gene: EIF2AK2 as Green List (high evidence)
Mendeliome v0.1842 EIF2AK2 Zornitza Stark Gene: eif2ak2 has been classified as Green List (High Evidence).
Mendeliome v0.1841 EIF2AK2 Zornitza Stark gene: EIF2AK2 was added
gene: EIF2AK2 was added to Mendeliome. Sources: Literature
Mode of inheritance for gene: EIF2AK2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: EIF2AK2 were set to 32197074
Phenotypes for gene: EIF2AK2 were set to Intellectual disability; white matter abnormalities; ataxia; regression with febrile illness
Review for gene: EIF2AK2 was set to GREEN
Added comment: Eight individuals with de novo variants and complex neurodevelopmental phenotype.
Sources: Literature
Intellectual disability syndromic and non-syndromic v0.2488 EIF2AK2 Zornitza Stark Classified gene: EIF2AK2 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2488 EIF2AK2 Zornitza Stark Gene: eif2ak2 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2487 EIF2AK2 Zornitza Stark gene: EIF2AK2 was added
gene: EIF2AK2 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature
Mode of inheritance for gene: EIF2AK2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: EIF2AK2 were set to 32197074
Phenotypes for gene: EIF2AK2 were set to Intellectual disability; white matter abnormalities; ataxia; regression with febrile illness
Review for gene: EIF2AK2 was set to GREEN
Added comment: Eight individuals with de novo variants and complex neurodevelopmental phenotype.
Sources: Literature
Mendeliome v0.1840 EIF2AK1 Zornitza Stark Marked gene: EIF2AK1 as ready
Mendeliome v0.1840 EIF2AK1 Zornitza Stark Gene: eif2ak1 has been classified as Red List (Low Evidence).
Mendeliome v0.1840 EIF2AK1 Zornitza Stark gene: EIF2AK1 was added
gene: EIF2AK1 was added to Mendeliome. Sources: Literature
Mode of inheritance for gene: EIF2AK1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: EIF2AK1 were set to 32197074
Phenotypes for gene: EIF2AK1 were set to Intellectual disability; white matter abnormalities
Review for gene: EIF2AK1 was set to RED
Added comment: Single individual reported with de novo variant in this gene.
Sources: Literature
Intellectual disability syndromic and non-syndromic v0.2486 EIF2AK1 Zornitza Stark Marked gene: EIF2AK1 as ready
Intellectual disability syndromic and non-syndromic v0.2486 EIF2AK1 Zornitza Stark Gene: eif2ak1 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2486 EIF2AK1 Zornitza Stark gene: EIF2AK1 was added
gene: EIF2AK1 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature
Mode of inheritance for gene: EIF2AK1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: EIF2AK1 were set to 32197074
Phenotypes for gene: EIF2AK1 were set to Intellectual disability; white matter abnormalities
Review for gene: EIF2AK1 was set to RED
Added comment: Single individual reported with de novo variant in this gene.
Sources: Literature
Mendeliome v0.1839 NOVA2 Zornitza Stark Marked gene: NOVA2 as ready
Mendeliome v0.1839 NOVA2 Zornitza Stark Gene: nova2 has been classified as Green List (High Evidence).
Mendeliome v0.1839 NOVA2 Zornitza Stark Classified gene: NOVA2 as Green List (high evidence)
Mendeliome v0.1839 NOVA2 Zornitza Stark Gene: nova2 has been classified as Green List (High Evidence).
Mendeliome v0.1838 NOVA2 Zornitza Stark gene: NOVA2 was added
gene: NOVA2 was added to Mendeliome. Sources: Literature
Mode of inheritance for gene: NOVA2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: NOVA2 were set to 32197073
Phenotypes for gene: NOVA2 were set to Intellectual disability; autism; hypotonia; spasticity; ataxia
Mode of pathogenicity for gene: NOVA2 was set to Other
Review for gene: NOVA2 was set to GREEN
Added comment: Six individuals with de novo frameshift variants resulting in C-terminal extension suggesting partial LoF as mechanism.
Sources: Literature
Intellectual disability syndromic and non-syndromic v0.2485 NOVA2 Zornitza Stark Marked gene: NOVA2 as ready
Intellectual disability syndromic and non-syndromic v0.2485 NOVA2 Zornitza Stark Gene: nova2 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2485 NOVA2 Zornitza Stark Classified gene: NOVA2 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2485 NOVA2 Zornitza Stark Gene: nova2 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2484 NOVA2 Zornitza Stark gene: NOVA2 was added
gene: NOVA2 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature
Mode of inheritance for gene: NOVA2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: NOVA2 were set to 32197073
Phenotypes for gene: NOVA2 were set to Intellectual disability; autism; hypotonia; spasticity; ataxia
Mode of pathogenicity for gene: NOVA2 was set to Other
Review for gene: NOVA2 was set to GREEN
Added comment: Six individuals with de novo frameshift variants resulting in C-terminal extension suggesting partial LoF as mechanism.
Sources: Literature
Early-onset Parkinson disease v0.23 PTS Bryony Thompson Mode of inheritance for gene: PTS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Early-onset Parkinson disease v0.22 PTS Bryony Thompson Marked gene: PTS as ready
Early-onset Parkinson disease v0.22 PTS Bryony Thompson Gene: pts has been classified as Green List (High Evidence).
Early-onset Parkinson disease v0.22 PTS Bryony Thompson reviewed gene: PTS: Rating: GREEN; Mode of pathogenicity: None; Publications: 11388593, 27562098; Phenotypes: Hyperphenylalaninemia, BH4-deficient, A MIM#261640; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early-onset Parkinson disease v0.22 PTRHD1 Bryony Thompson Marked gene: PTRHD1 as ready
Early-onset Parkinson disease v0.22 PTRHD1 Bryony Thompson Gene: ptrhd1 has been classified as Green List (High Evidence).
Early-onset Parkinson disease v0.22 PTRHD1 Bryony Thompson Classified gene: PTRHD1 as Green List (high evidence)
Early-onset Parkinson disease v0.22 PTRHD1 Bryony Thompson Gene: ptrhd1 has been classified as Green List (High Evidence).
Early-onset Parkinson disease v0.21 PTRHD1 Bryony Thompson gene: PTRHD1 was added
gene: PTRHD1 was added to Early onset Parkinson disease. Sources: Expert list
Mode of inheritance for gene: PTRHD1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PTRHD1 were set to 27753167; 27134041; 30398675; 29143421
Phenotypes for gene: PTRHD1 were set to early-onset parkinsonism; intellectual disability
Review for gene: PTRHD1 was set to GREEN
Added comment: Homozygous variants segregate in three unrelated families from Iran and South Africa. No functional assays conducted.
Sources: Expert list
Early-onset Parkinson disease v0.20 KIF5A Bryony Thompson Marked gene: KIF5A as ready
Early-onset Parkinson disease v0.20 KIF5A Bryony Thompson Gene: kif5a has been classified as Amber List (Moderate Evidence).
Early-onset Parkinson disease v0.20 KIF5A Bryony Thompson Classified gene: KIF5A as Amber List (moderate evidence)
Early-onset Parkinson disease v0.20 KIF5A Bryony Thompson Gene: kif5a has been classified as Amber List (Moderate Evidence).
Early-onset Parkinson disease v0.19 KIF5A Bryony Thompson reviewed gene: KIF5A: Rating: AMBER; Mode of pathogenicity: None; Publications: 18853458; Phenotypes: Spastic paraplegia 10, autosomal dominant MIM#604187; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early-onset Parkinson disease v0.19 C9orf72 Bryony Thompson Classified gene: C9orf72 as Red List (low evidence)
Early-onset Parkinson disease v0.19 C9orf72 Bryony Thompson Added comment: Comment on list classification: A repeat expansion is the cause of disease for this gene, which is currently not detectable by NGS.
Early-onset Parkinson disease v0.19 C9orf72 Bryony Thompson Gene: c9orf72 has been classified as Red List (Low Evidence).
Early-onset Parkinson disease v0.18 C9orf72 Bryony Thompson changed review comment from: Comment on list classification: A repeat expansion is the cause of disease for this gene, which is currently not detectable by NGS.; to: Parkinsonism is a common feature of the condition. A repeat expansion is the cause of disease for this gene.
Early-onset Parkinson disease v0.18 C9orf72 Bryony Thompson changed review comment from: Comment on list classification: A repeat expansion is the cause of disease for this gene, which is currently not detectable by NGS.; to: Comment on list classification: A repeat expansion is the cause of disease for this gene, which is currently not detectable by NGS.
Early-onset Parkinson disease v0.18 C9orf72 Bryony Thompson edited their review of gene: C9orf72: Changed rating: GREEN; Changed publications: 31779815; Changed phenotypes: Frontotemporal dementia and/or amyotrophic lateral sclerosis 1 MIM#105550; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early-onset Parkinson disease v0.18 HTT Bryony Thompson Marked gene: HTT as ready
Early-onset Parkinson disease v0.18 HTT Bryony Thompson Gene: htt has been classified as Red List (Low Evidence).
Early-onset Parkinson disease v0.18 HTT Bryony Thompson Classified gene: HTT as Red List (low evidence)
Early-onset Parkinson disease v0.18 HTT Bryony Thompson Added comment: Comment on list classification: Parkinsonism is a feature of Huntingtons. This repeat expansion is not detectable by current NGS technology.
Early-onset Parkinson disease v0.18 HTT Bryony Thompson Gene: htt has been classified as Red List (Low Evidence).
Early-onset Parkinson disease v0.17 HTT Bryony Thompson Tag STR tag was added to gene: HTT.
Early-onset Parkinson disease v0.17 HTT Bryony Thompson reviewed gene: HTT: Rating: GREEN; Mode of pathogenicity: None; Publications: 26740508, 27329733, 31800013; Phenotypes: Lopes-Maciel-Rodan syndrome MIM#617435, Huntington disease MIM#143100; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Genetic Epilepsy v0.640 NRROS Zornitza Stark Marked gene: NRROS as ready
Genetic Epilepsy v0.640 NRROS Zornitza Stark Gene: nrros has been classified as Green List (High Evidence).
Genetic Epilepsy v0.640 NRROS Zornitza Stark Classified gene: NRROS as Green List (high evidence)
Genetic Epilepsy v0.640 NRROS Zornitza Stark Gene: nrros has been classified as Green List (High Evidence).
Genetic Epilepsy v0.639 NRROS Zornitza Stark reviewed gene: NRROS: Rating: GREEN; Mode of pathogenicity: None; Publications: 32100099, 32197075; Phenotypes: neurodegeneration, intracranial calcification, epilepsy; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Brain Calcification v0.16 NRROS Zornitza Stark Marked gene: NRROS as ready
Brain Calcification v0.16 NRROS Zornitza Stark Gene: nrros has been classified as Green List (High Evidence).
Brain Calcification v0.16 NRROS Zornitza Stark Classified gene: NRROS as Green List (high evidence)
Brain Calcification v0.16 NRROS Zornitza Stark Gene: nrros has been classified as Green List (High Evidence).
Brain Calcification v0.15 NRROS Zornitza Stark gene: NRROS was added
gene: NRROS was added to Brain Calcification. Sources: Literature
Mode of inheritance for gene: NRROS was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NRROS were set to 32100099; 32197075
Phenotypes for gene: NRROS were set to neurodegeneration; intracranial calcification; epilepsy
Review for gene: NRROS was set to GREEN
Added comment: Normal development or mild developmental delay until onset of regression around age of 1 concurrent with epilepsy
Biallelic LOF mutations with functional evidence of pathogenicity reported in 6 unrelated families.
Sources: Literature
Early-onset Parkinson disease v0.17 FMR1 Bryony Thompson Marked gene: FMR1 as ready
Early-onset Parkinson disease v0.17 FMR1 Bryony Thompson Gene: fmr1 has been classified as Green List (High Evidence).
Early-onset Parkinson disease v0.17 FMR1 Bryony Thompson Tag STR tag was added to gene: FMR1.
Early-onset Parkinson disease v0.17 FMR1 Bryony Thompson reviewed gene: FMR1: Rating: GREEN; Mode of pathogenicity: None; Publications: 27340021, 28176767; Phenotypes: Fragile X tremor/ataxia syndrome MIM#300623, Fragile X syndrome MIM#300624; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Mendeliome v0.1837 GNB2 Sue White Classified gene: GNB2 as Amber List (moderate evidence)
Mendeliome v0.1837 GNB2 Sue White Gene: gnb2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1836 GNB2 Sue White gene: GNB2 was added
gene: GNB2 was added to Mendeliome. Sources: Literature
Mode of inheritance for gene: GNB2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: GNB2 were set to 31698099
Phenotypes for gene: GNB2 were set to intellectual disability; dysmorphic features
Penetrance for gene: GNB2 were set to Complete
Review for gene: GNB2 was set to AMBER
Added comment: single report of patient with de novo missense variant in GNB2 and intellectual disability. Emerging evidence of other de no missense variants in GNB2 and ID
Sources: Literature
Intellectual disability syndromic and non-syndromic v0.2483 GNB2 Sue White Classified gene: GNB2 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2483 GNB2 Sue White Gene: gnb2 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2482 GNB2 Sue White gene: GNB2 was added
gene: GNB2 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature
Mode of inheritance for gene: GNB2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: GNB2 were set to 31698099
Phenotypes for gene: GNB2 were set to intellectual disability; dysmorphic features
Review for gene: GNB2 was set to AMBER
Added comment: emerging evidence of de novo missense variants in patients with intellectual disability
Sources: Literature
Mendeliome v0.1835 NRROS Sue White Classified gene: NRROS as Green List (high evidence)
Mendeliome v0.1835 NRROS Sue White Gene: nrros has been classified as Green List (High Evidence).
Mendeliome v0.1834 NRROS Sue White gene: NRROS was added
gene: NRROS was added to Mendeliome. Sources: Literature
Mode of inheritance for gene: NRROS was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NRROS were set to 32100099; 32197075
Phenotypes for gene: NRROS were set to neurodegeneration; intracranial calcification; epilepsy
Penetrance for gene: NRROS were set to Complete
Review for gene: NRROS was set to GREEN
Added comment: normal development or mild developmental delay until onset of regression around age of 1 concurrent with epilepsy
biallelic LOF mutations with functional evidence of pathogenicity
Sources: Literature
Genetic Epilepsy v0.639 NRROS Sue White gene: NRROS was added
gene: NRROS was added to Genetic Epilepsy. Sources: Literature
Mode of inheritance for gene: NRROS was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NRROS were set to 32100099; 32197075
Phenotypes for gene: NRROS were set to neurodegeneration; intracranial calcification; epilepsy
Penetrance for gene: NRROS were set to Complete
Regression v0.96 NRROS Sue White Classified gene: NRROS as Green List (high evidence)
Regression v0.96 NRROS Sue White Gene: nrros has been classified as Green List (High Evidence).
Regression v0.95 NRROS Sue White gene: NRROS was added
gene: NRROS was added to Regression. Sources: Literature
Mode of inheritance for gene: NRROS was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NRROS were set to 32100099
Phenotypes for gene: NRROS were set to neurodegeneration; intracranial calcification; epilepsy
Penetrance for gene: NRROS were set to Complete
Review for gene: NRROS was set to GREEN
Added comment: Sources: Literature
Intellectual disability syndromic and non-syndromic v0.2481 NRROS Sue White Classified gene: NRROS as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2481 NRROS Sue White Gene: nrros has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2480 NRROS Sue White gene: NRROS was added
gene: NRROS was added to Intellectual disability syndromic and non-syndromic. Sources: Literature
Mode of inheritance for gene: NRROS was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NRROS were set to 32197075; 32100099
Phenotypes for gene: NRROS were set to neurodegeneration; intracranial calcification; epilepsy
Penetrance for gene: NRROS were set to Complete
Review for gene: NRROS was set to GREEN
Added comment: Sources: Literature
Early-onset Parkinson disease v0.17 TMEM230 Bryony Thompson gene: TMEM230 was added
gene: TMEM230 was added to Early onset Parkinson disease. Sources: Expert list
Mode of inheritance for gene: TMEM230 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: TMEM230 were set to 30804554; 27270108; 28115417; 28017548; 30804555; 30804556; 31323517
Phenotypes for gene: TMEM230 were set to Parkinson disease 21, MIM#616361
Review for gene: TMEM230 was set to AMBER
Added comment: A single family segregating a heterozygous missense (p.Arg141Leu) and supporting functional evidence. However, another group found a DNAJC13 variant in the same family also with supporting functional evidence. A stoploss was also identified in 9 Chinese Parkinson disease probands, however it was identified homozygous in 7 of these with no difference in the severity of phenotype. A similar stop loss was identified in a North American PD case. Another missense was identified in an apparently sporadic PD case (p.Tyr92Cys), but was also present in the unaffected mother (age 57 yrs). Another rare missense has been reported in a case with familial PD. The missense reported in a family from Southern Italy is too common in gnomAD v2.1 for a dominant disease (PMID: 31323517 - p.Ile125Met).
Sources: Expert list
Autism v0.80 CNOT3 Zornitza Stark Marked gene: CNOT3 as ready
Autism v0.80 CNOT3 Zornitza Stark Gene: cnot3 has been classified as Green List (High Evidence).
Autism v0.80 CNOT3 Zornitza Stark Phenotypes for gene: CNOT3 were changed from to Intellectual developmental disorder with speech delay, autism, and dysmorphic facies, MIM# 618672
Autism v0.79 CNOT3 Zornitza Stark Publications for gene: CNOT3 were set to
Autism v0.78 CNOT3 Zornitza Stark Mode of inheritance for gene: CNOT3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Autism v0.77 CNOT3 Zornitza Stark reviewed gene: CNOT3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31201375; Phenotypes: Intellectual developmental disorder with speech delay, autism, and dysmorphic facies, MIM# 618672; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1833 CNOT3 Zornitza Stark Marked gene: CNOT3 as ready
Mendeliome v0.1833 CNOT3 Zornitza Stark Gene: cnot3 has been classified as Green List (High Evidence).
Mendeliome v0.1833 CNOT3 Zornitza Stark Phenotypes for gene: CNOT3 were changed from to Intellectual developmental disorder with speech delay, autism, and dysmorphic facies, MIM# 618672
Intellectual disability syndromic and non-syndromic v0.2479 CNOT3 Zornitza Stark Marked gene: CNOT3 as ready
Intellectual disability syndromic and non-syndromic v0.2479 CNOT3 Zornitza Stark Added comment: Comment when marking as ready: 16 unrelated individuals reported.
Intellectual disability syndromic and non-syndromic v0.2479 CNOT3 Zornitza Stark Gene: cnot3 has been classified as Green List (High Evidence).
Mendeliome v0.1832 CNOT3 Zornitza Stark Publications for gene: CNOT3 were set to
Mendeliome v0.1831 CNOT3 Zornitza Stark Mode of inheritance for gene: CNOT3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1830 CNOT3 Zornitza Stark reviewed gene: CNOT3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31201375; Phenotypes: Intellectual developmental disorder with speech delay, autism, and dysmorphic facies, MIM# 618672; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2479 CNOT3 Zornitza Stark Marked gene: CNOT3 as ready
Intellectual disability syndromic and non-syndromic v0.2479 CNOT3 Zornitza Stark Gene: cnot3 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2479 CNOT3 Zornitza Stark Phenotypes for gene: CNOT3 were changed from to Intellectual developmental disorder with speech delay, autism, and dysmorphic facies 618672
Intellectual disability syndromic and non-syndromic v0.2478 CNOT3 Zornitza Stark Publications for gene: CNOT3 were set to
Intellectual disability syndromic and non-syndromic v0.2477 CNOT3 Zornitza Stark Mode of inheritance for gene: CNOT3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2476 CNOT3 Teresa Zhao reviewed gene: CNOT3: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 31201375; Phenotypes: Intellectual developmental disorder with speech delay, autism, and dysmorphic facies 618672; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early-onset Parkinson disease v0.16 DNAJC13 Bryony Thompson Marked gene: DNAJC13 as ready
Early-onset Parkinson disease v0.16 DNAJC13 Bryony Thompson Gene: dnajc13 has been classified as Red List (Low Evidence).
Early-onset Parkinson disease v0.16 DNAJC13 Bryony Thompson edited their review of gene: DNAJC13: Changed phenotypes: Parkinson disease 21, MIM#616361
Early-onset Parkinson disease v0.16 DNAJC13 Bryony Thompson gene: DNAJC13 was added
gene: DNAJC13 was added to Early onset Parkinson disease. Sources: Expert list
Mode of inheritance for gene: DNAJC13 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: DNAJC13 were set to 30788857; 24218364; 29309590; 31082451; 29887357; 27270108
Review for gene: DNAJC13 was set to AMBER
Added comment: A single family segregating a heterozygous missense (p.Asn855Ser) and supporting functional evidence. However, another group found a TMEM230 variant in the same family also with supporting functional evidence. Two missense reported in two other studies (PMID: 30788857 - p.Arg1382His; PMID: 29887357 - p.Arg903Lys) are more common in gnomAD v2.1 than would be expected for a dominant disorder.
Sources: Expert list
Early-onset Parkinson disease v0.15 DCAF17 Bryony Thompson Marked gene: DCAF17 as ready
Early-onset Parkinson disease v0.15 DCAF17 Bryony Thompson Gene: dcaf17 has been classified as Red List (Low Evidence).
Early-onset Parkinson disease v0.15 DCAF17 Bryony Thompson Classified gene: DCAF17 as Red List (low evidence)
Early-onset Parkinson disease v0.15 DCAF17 Bryony Thompson Added comment: Comment on list classification: Dystonia rather parkinsonism appears to be a feature of this condition and this gene is one the dystonia panel.
Early-onset Parkinson disease v0.15 DCAF17 Bryony Thompson Gene: dcaf17 has been classified as Red List (Low Evidence).
Early-onset Parkinson disease v0.14 DCAF17 Bryony Thompson reviewed gene: DCAF17: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Woodhouse-Sakati syndrome MIM#241080; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early-onset Parkinson disease v0.14 ATP7B Bryony Thompson Marked gene: ATP7B as ready
Early-onset Parkinson disease v0.14 ATP7B Bryony Thompson Gene: atp7b has been classified as Green List (High Evidence).
Early-onset Parkinson disease v0.14 ATP7B Bryony Thompson Classified gene: ATP7B as Green List (high evidence)
Early-onset Parkinson disease v0.14 ATP7B Bryony Thompson Gene: atp7b has been classified as Green List (High Evidence).
Early-onset Parkinson disease v0.13 ATP7B Bryony Thompson gene: ATP7B was added
gene: ATP7B was added to Early onset Parkinson disease. Sources: Expert list
Mode of inheritance for gene: ATP7B was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ATP7B were set to 17435591
Phenotypes for gene: ATP7B were set to Wilson disease MIM#277900
Review for gene: ATP7B was set to GREEN
Added comment: Parkinsonism is a prominent neurological feature of Wilson disease.
Sources: Expert list
Early-onset Parkinson disease v0.12 CP Bryony Thompson reviewed gene: CP: Rating: GREEN; Mode of pathogenicity: None; Publications: 28012953; Phenotypes: Hemosiderosis, systemic, due to aceruloplasminemia MIM#604290; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early-onset Parkinson disease v0.12 CLN3 Bryony Thompson reviewed gene: CLN3: Rating: GREEN; Mode of pathogenicity: None; Publications: 19489875, 11342698; Phenotypes: Ceroid lipofuscinosis, neuronal, 3 MIM#204200; Mode of inheritance: None
Early-onset Parkinson disease v0.12 CHCHD2 Bryony Thompson edited their review of gene: CHCHD2: Changed publications: 32068847, 25662902, 31600778, 26705026
Incidentalome v0.12 CHCHD2 Bryony Thompson Publications for gene: CHCHD2 were set to 32068847; 25662902; 31600778
Early-onset Parkinson disease v0.12 CHCHD2 Bryony Thompson Publications for gene: CHCHD2 were set to 32068847; 25662902; 31600778
Incidentalome v0.11 CHCHD2 Bryony Thompson Classified gene: CHCHD2 as Green List (high evidence)
Incidentalome v0.11 CHCHD2 Bryony Thompson Gene: chchd2 has been classified as Green List (High Evidence).
Incidentalome v0.10 CHCHD2 Bryony Thompson gene: CHCHD2 was added
gene: CHCHD2 was added to Incidentalome. Sources: Expert list
Mode of inheritance for gene: CHCHD2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CHCHD2 were set to 32068847; 25662902; 31600778
Phenotypes for gene: CHCHD2 were set to Parkinson disease 22, autosomal dominant MIM#616710
Review for gene: CHCHD2 was set to GREEN
Added comment: Adult-onset neurodegenerative disorder. Five families with heterozygous variants, segregation evidence for T61I in multiple families. Supporting functional evidence suggesting mitochondrial dysfunction through the genes role in mitochondrial respiratory function.
Sources: Expert list
Mitochondrial disease v0.322 CHCHD2 Bryony Thompson Classified gene: CHCHD2 as Green List (high evidence)
Mitochondrial disease v0.322 CHCHD2 Bryony Thompson Gene: chchd2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.321 CHCHD2 Bryony Thompson gene: CHCHD2 was added
gene: CHCHD2 was added to Mitochondrial disease. Sources: Literature
Mode of inheritance for gene: CHCHD2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CHCHD2 were set to 32068847; 25662902; 31600778
Phenotypes for gene: CHCHD2 were set to Parkinson disease 22, autosomal dominant MIM#616710
Review for gene: CHCHD2 was set to GREEN
Added comment: Five families with heterozygous variants, segregation evidence for T61I in multiple families. Supporting functional evidence suggesting mitochondrial dysfunction through the genes role in mitochondrial respiratory function.
Sources: Literature
Early-onset Parkinson disease v0.11 CHCHD2 Bryony Thompson Classified gene: CHCHD2 as Green List (high evidence)
Early-onset Parkinson disease v0.11 CHCHD2 Bryony Thompson Gene: chchd2 has been classified as Green List (High Evidence).
Early-onset Parkinson disease v0.10 CHCHD2 Bryony Thompson gene: CHCHD2 was added
gene: CHCHD2 was added to Early onset Parkinson disease. Sources: Expert list
Mode of inheritance for gene: CHCHD2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CHCHD2 were set to 32068847; 25662902; 31600778
Phenotypes for gene: CHCHD2 were set to Parkinson disease 22, autosomal dominant MIM#616710
Review for gene: CHCHD2 was set to GREEN
Added comment: Five families with heterozygous variants, segregation evidence for T61I in multiple families. Supporting functional evidence suggesting mitochondrial dysfunction through the genes role in mitochondrial respiratory function.
Sources: Expert list
Early-onset Parkinson disease v0.9 C9orf72 Bryony Thompson Classified gene: C9orf72 as Red List (low evidence)
Early-onset Parkinson disease v0.9 C9orf72 Bryony Thompson Added comment: Comment on list classification: A repeat expansion is the cause of disease for this gene, which is currently not detectable by NGS.
Early-onset Parkinson disease v0.9 C9orf72 Bryony Thompson Gene: c9orf72 has been classified as Red List (Low Evidence).
Early-onset Parkinson disease v0.8 C9orf72 Bryony Thompson Tag STR tag was added to gene: C9orf72.
Early-onset Parkinson disease v0.8 AFG3L2 Bryony Thompson Marked gene: AFG3L2 as ready
Early-onset Parkinson disease v0.8 AFG3L2 Bryony Thompson Gene: afg3l2 has been classified as Red List (Low Evidence).
Early-onset Parkinson disease v0.8 AFG3L2 Bryony Thompson Classified gene: AFG3L2 as Red List (low evidence)
Early-onset Parkinson disease v0.8 AFG3L2 Bryony Thompson Gene: afg3l2 has been classified as Red List (Low Evidence).
Early-onset Parkinson disease v0.7 AFG3L2 Bryony Thompson reviewed gene: AFG3L2: Rating: RED; Mode of pathogenicity: None; Publications: 30252181; Phenotypes: optic atrophy, spastic ataxia, L-dopa-responsive parkinsonism; Mode of inheritance: Unknown
Mendeliome v0.1830 CBS Zornitza Stark Marked gene: CBS as ready
Mendeliome v0.1830 CBS Zornitza Stark Gene: cbs has been classified as Green List (High Evidence).
Mendeliome v0.1830 CBS Zornitza Stark Phenotypes for gene: CBS were changed from to Homocystinuria, B6-responsive and nonresponsive types, 236200; Thrombosis, hyperhomocysteinemic, 236200
Mendeliome v0.1829 CBS Zornitza Stark Publications for gene: CBS were set to
Mendeliome v0.1828 CBS Zornitza Stark Mode of inheritance for gene: CBS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Skeletal dysplasia v0.11 FLNB Zornitza Stark Marked gene: FLNB as ready
Skeletal dysplasia v0.11 FLNB Zornitza Stark Gene: flnb has been classified as Green List (High Evidence).
Skeletal dysplasia v0.11 FLNB Zornitza Stark Publications for gene: FLNB were set to
Skeletal dysplasia v0.10 FLNB Chern Lim reviewed gene: FLNB: Rating: GREEN; Mode of pathogenicity: Other; Publications: 22190451, 29566257; Phenotypes: Atelosteogenesis, type I AD MIM#108720, Atelosteogenesis, type III AD MIM#108721, Boomerang dysplasia AD MIM#112310, Larsen syndrome AD MIM#150250, Spondylocarpotarsal synostosis syndrome AR MIM#272460; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Retinitis pigmentosa_Autosomal Recessive/X-linked v0.18 POC5 Bryony Thompson Marked gene: POC5 as ready
Retinitis pigmentosa_Autosomal Recessive/X-linked v0.18 POC5 Bryony Thompson Gene: poc5 has been classified as Amber List (Moderate Evidence).
Retinitis pigmentosa_Autosomal Recessive/X-linked v0.18 POC5 Bryony Thompson Classified gene: POC5 as Amber List (moderate evidence)
Retinitis pigmentosa_Autosomal Recessive/X-linked v0.18 POC5 Bryony Thompson Gene: poc5 has been classified as Amber List (Moderate Evidence).
Retinitis pigmentosa_Autosomal Recessive/X-linked v0.17 POC5 Bryony Thompson gene: POC5 was added
gene: POC5 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa. Sources: Expert list
Mode of inheritance for gene: POC5 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: POC5 were set to 29272404
Phenotypes for gene: POC5 were set to retinitis pigmentosa; short stature; microcephaly; recurrent glomerulonephritis
Review for gene: POC5 was set to AMBER
Added comment: One case with a homozygous truncating variant and a supporting zebrafish model.
Sources: Expert list
Syndromic Retinopathy v0.6 POC5 Bryony Thompson Marked gene: POC5 as ready
Syndromic Retinopathy v0.6 POC5 Bryony Thompson Gene: poc5 has been classified as Amber List (Moderate Evidence).
Syndromic Retinopathy v0.6 POC5 Bryony Thompson Classified gene: POC5 as Amber List (moderate evidence)
Syndromic Retinopathy v0.6 POC5 Bryony Thompson Gene: poc5 has been classified as Amber List (Moderate Evidence).
Syndromic Retinopathy v0.5 POC5 Bryony Thompson reviewed gene: POC5: Rating: AMBER; Mode of pathogenicity: None; Publications: 29272404; Phenotypes: retinitis pigmentosa, short stature, microcephaly, recurrent glomerulonephritis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1827 CBS Kristin Rigbye reviewed gene: CBS: Rating: GREEN; Mode of pathogenicity: None; Publications: 7506602, 10338090; Phenotypes: Homocystinuria, B6-responsive and nonresponsive types, 236200, Thrombosis, hyperhomocysteinemic, 236200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Bardet Biedl syndrome v0.24 Bryony Thompson Panel types changed to Victorian Clinical Genetics Services; Royal Melbourne Hospital; Rare Disease
Hereditary Neuropathy_CMT - isolated v0.8 Bryony Thompson Panel name changed from Hereditary Neuropathy - isolated_RMH to Hereditary Neuropathy - isolated
Panel types changed to Royal Melbourne Hospital; Rare Disease
Hereditary Neuropathy_CMT - isolated v0.7 SCO2 Bryony Thompson reviewed gene: SCO2: Rating: AMBER; Mode of pathogenicity: None; Publications: 29351582; Phenotypes: axonal Charcot-Marie-Tooth disease; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary Neuropathy_CMT - isolated v0.7 NAGLU Bryony Thompson Marked gene: NAGLU as ready
Hereditary Neuropathy_CMT - isolated v0.7 NAGLU Bryony Thompson Gene: naglu has been classified as Amber List (Moderate Evidence).
Hereditary Neuropathy_CMT - isolated v0.7 NAGLU Bryony Thompson reviewed gene: NAGLU: Rating: AMBER; Mode of pathogenicity: None; Publications: 25818867; Phenotypes: Charcot-Marie-Tooth disease, axonal, type 2V MIM#616491; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cataract v0.60 FOXP3 Zornitza Stark Marked gene: FOXP3 as ready
Cataract v0.60 FOXP3 Zornitza Stark Gene: foxp3 has been classified as Red List (Low Evidence).
Cataract v0.60 FOXP3 Zornitza Stark Phenotypes for gene: FOXP3 were changed from to Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, 304790
Cataract v0.59 FOXP3 Zornitza Stark Mode of inheritance for gene: FOXP3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Cataract v0.58 FOXP3 Zornitza Stark Classified gene: FOXP3 as Red List (low evidence)
Cataract v0.58 FOXP3 Zornitza Stark Gene: foxp3 has been classified as Red List (Low Evidence).
Cataract v0.57 GUCY2C Zornitza Stark Marked gene: GUCY2C as ready
Cataract v0.57 GUCY2C Zornitza Stark Gene: gucy2c has been classified as Red List (Low Evidence).
Cataract v0.57 GUCY2C Zornitza Stark Phenotypes for gene: GUCY2C were changed from to Diarrhea 6, 614616; Meconium ileus, 614665
Cataract v0.56 GUCY2C Zornitza Stark Classified gene: GUCY2C as Red List (low evidence)
Cataract v0.56 GUCY2C Zornitza Stark Gene: gucy2c has been classified as Red List (Low Evidence).
Hereditary Neuropathy_CMT - isolated v0.7 KIF1B Bryony Thompson Marked gene: KIF1B as ready
Hereditary Neuropathy_CMT - isolated v0.7 KIF1B Bryony Thompson Gene: kif1b has been classified as Amber List (Moderate Evidence).
Hereditary Neuropathy_CMT - isolated v0.7 KIF1B Bryony Thompson reviewed gene: KIF1B: Rating: AMBER; Mode of pathogenicity: None; Publications: 11389829, 30126838, 25802885; Phenotypes: Charcot-Marie-Tooth disease, type 2A1 MIM#118210; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary Neuropathy_CMT - isolated v0.7 DGAT2 Bryony Thompson reviewed gene: DGAT2: Rating: AMBER; Mode of pathogenicity: None; Publications: 26786738; Phenotypes: axonal Charcot-Marie-Tooth disease; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary Neuropathy_CMT - isolated v0.7 SH3BP4 Bryony Thompson reviewed gene: SH3BP4: Rating: RED; Mode of pathogenicity: None; Publications: 24627108; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Hereditary Neuropathy_CMT - isolated v0.7 KLHL13 Bryony Thompson reviewed gene: KLHL13: Rating: RED; Mode of pathogenicity: None; Publications: 24627108; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Hereditary Neuropathy_CMT - isolated v0.7 UBA1 Bryony Thompson Classified gene: UBA1 as Green List (high evidence)
Hereditary Neuropathy_CMT - isolated v0.7 UBA1 Bryony Thompson Gene: uba1 has been classified as Green List (High Evidence).
Hereditary Neuropathy_CMT - isolated v0.6 UBA1 Bryony Thompson Deleted their comment
Hereditary Neuropathy_CMT - isolated v0.6 UBA1 Bryony Thompson edited their review of gene: UBA1: Added comment: Five families reported. Children with XL-SMA usually die from respiratory failure by age two years; however, the age at death ranges from the neonatal period to adolescence, the latter in those exceptional cases in which extensive respiratory and medical support are provided (genereviews).; Changed rating: GREEN; Changed publications: 18179898; Changed phenotypes: Spinal muscular atrophy, X-linked 2, infantile MIM#301830; Changed mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Hereditary Neuropathy - complex v0.14 Bryony Thompson Panel name changed from Hereditary Neuropathy - complex_RMH to Hereditary Neuropathy - complex
Panel types changed to Royal Melbourne Hospital; Rare Disease
Hereditary Neuropathy - complex v0.13 PEX12 Bryony Thompson reviewed gene: PEX12: Rating: RED; Mode of pathogenicity: None; Publications: 24627108; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary Neuropathy - complex v0.13 NIPA1 Bryony Thompson reviewed gene: NIPA1: Rating: RED; Mode of pathogenicity: None; Publications: 21419568; Phenotypes: Spastic paraplegia 6, autosomal dominant MIM#600363; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary Neuropathy - complex v0.13 IFRD1 Bryony Thompson reviewed gene: IFRD1: Rating: RED; Mode of pathogenicity: None; Publications: 29362493, 19409521; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1827 HTR3C Zornitza Stark Marked gene: HTR3C as ready
Mendeliome v0.1827 HTR3C Zornitza Stark Added comment: Comment when marking as ready: Agree no evidence for Mendelian gene-disease association currently.
Mendeliome v0.1827 HTR3C Zornitza Stark Gene: htr3c has been classified as Red List (Low Evidence).
Mendeliome v0.1827 HTR3C Zornitza Stark Publications for gene: HTR3C were set to
Mendeliome v0.1826 HTR3C Zornitza Stark Classified gene: HTR3C as Red List (low evidence)
Mendeliome v0.1826 HTR3C Zornitza Stark Gene: htr3c has been classified as Red List (Low Evidence).
Mendeliome v0.1825 ZFP42 Zornitza Stark Marked gene: ZFP42 as ready
Mendeliome v0.1825 ZFP42 Zornitza Stark Gene: zfp42 has been classified as Red List (Low Evidence).
Mendeliome v0.1825 ZFP42 Zornitza Stark Classified gene: ZFP42 as Red List (low evidence)
Mendeliome v0.1825 ZFP42 Zornitza Stark Gene: zfp42 has been classified as Red List (Low Evidence).
Cataract v0.55 CYBA Zornitza Stark Marked gene: CYBA as ready
Cataract v0.55 CYBA Zornitza Stark Gene: cyba has been classified as Red List (Low Evidence).
Cataract v0.55 CYBA Zornitza Stark Phenotypes for gene: CYBA were changed from to Chronic granulomatous disease
Cataract v0.54 GUCY2C Lauren Akesson commented on gene: GUCY2C: Cataract does not appear to be a typical feature in these conditions (OMIM)
Cataract v0.54 CYBA Zornitza Stark Mode of inheritance for gene: CYBA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Cataract v0.53 GUCY2C Lauren Akesson edited their review of gene: GUCY2C: Changed rating: RED
Cataract v0.53 CYBA Zornitza Stark Classified gene: CYBA as Red List (low evidence)
Cataract v0.53 CYBA Zornitza Stark Gene: cyba has been classified as Red List (Low Evidence).
Cataract v0.52 GUCY2C Lauren Akesson reviewed gene: GUCY2C: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: Diarrhea 6, 614616, Meconium ileus, 614665; Mode of inheritance: None
Cataract v0.52 CYBB Zornitza Stark Marked gene: CYBB as ready
Cataract v0.52 CYBB Zornitza Stark Gene: cybb has been classified as Red List (Low Evidence).
Cataract v0.52 CYBB Zornitza Stark Phenotypes for gene: CYBB were changed from to Chronic granulomatous disease; immunodeficiency 34 with mycobacteriosis
Cataract v0.51 CYBB Zornitza Stark Mode of inheritance for gene: CYBB was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Hereditary Neuropathy - complex v0.13 GJB3 Bryony Thompson Marked gene: GJB3 as ready
Hereditary Neuropathy - complex v0.13 GJB3 Bryony Thompson Gene: gjb3 has been classified as Red List (Low Evidence).
Hereditary Neuropathy - complex v0.13 GJB3 Bryony Thompson reviewed gene: GJB3: Rating: RED; Mode of pathogenicity: None; Publications: 11309368, 19755382, 16077902, 17142249, 12165562; Phenotypes: ; Mode of inheritance: None
Cataract v0.50 CYBB Zornitza Stark Classified gene: CYBB as Red List (low evidence)
Cataract v0.50 CYBB Zornitza Stark Gene: cybb has been classified as Red List (Low Evidence).
Cataract v0.49 DCLRE1C Zornitza Stark Marked gene: DCLRE1C as ready
Cataract v0.49 DCLRE1C Zornitza Stark Gene: dclre1c has been classified as Red List (Low Evidence).
Cataract v0.49 DCLRE1C Zornitza Stark Phenotypes for gene: DCLRE1C were changed from to Omenn syndrome 603554; Severe combined immunodeficiency, Athabascan type 602450
Cataract v0.48 DCLRE1C Zornitza Stark Mode of inheritance for gene: DCLRE1C was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Cataract v0.47 DCLRE1C Zornitza Stark Classified gene: DCLRE1C as Red List (low evidence)
Cataract v0.47 DCLRE1C Zornitza Stark Gene: dclre1c has been classified as Red List (Low Evidence).
Cataract v0.46 DOCK8 Zornitza Stark Marked gene: DOCK8 as ready
Cataract v0.46 DOCK8 Zornitza Stark Gene: dock8 has been classified as Red List (Low Evidence).
Cataract v0.46 DOCK8 Zornitza Stark Phenotypes for gene: DOCK8 were changed from to Hyper-IgE recurrent infection syndrome 243700
Cataract v0.45 DOCK8 Zornitza Stark Publications for gene: DOCK8 were set to
Cataract v0.44 DOCK8 Zornitza Stark Mode of inheritance for gene: DOCK8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Cataract v0.43 DOCK8 Zornitza Stark Tag SV/CNV tag was added to gene: DOCK8.
Cataract v0.43 DOCK8 Zornitza Stark Classified gene: DOCK8 as Red List (low evidence)
Cataract v0.43 DOCK8 Zornitza Stark Gene: dock8 has been classified as Red List (Low Evidence).
Cataract v0.42 EED Zornitza Stark Marked gene: EED as ready
Cataract v0.42 EED Zornitza Stark Added comment: Comment when marking as ready: Single individual reported, unclear at present whether this a feature of the phenotype or a coincidence.
Cataract v0.42 EED Zornitza Stark Gene: eed has been classified as Red List (Low Evidence).
Cataract v0.42 EED Zornitza Stark Classified gene: EED as Red List (low evidence)
Cataract v0.42 EED Zornitza Stark Gene: eed has been classified as Red List (Low Evidence).
Cataract v0.41 EPCAM Zornitza Stark Marked gene: EPCAM as ready
Cataract v0.41 EPCAM Zornitza Stark Gene: epcam has been classified as Red List (Low Evidence).
Cataract v0.41 EPCAM Zornitza Stark Phenotypes for gene: EPCAM were changed from to Congenital diarrhoea 5 with tufting enteropathy; Lynch syndrome
Cataract v0.40 FOXP3 Lauren Akesson reviewed gene: FOXP3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, 304790; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Cataract v0.40 EPCAM Zornitza Stark Publications for gene: EPCAM were set to
Cataract v0.39 EPCAM Zornitza Stark Mode of inheritance for gene: EPCAM was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cataract v0.38 EPCAM Zornitza Stark Classified gene: EPCAM as Red List (low evidence)
Cataract v0.38 EPCAM Zornitza Stark Gene: epcam has been classified as Red List (Low Evidence).
Cataract v0.37 FKRP Zornitza Stark Marked gene: FKRP as ready
Cataract v0.37 FKRP Zornitza Stark Gene: fkrp has been classified as Amber List (Moderate Evidence).
Cataract v0.37 FKRP Zornitza Stark Phenotypes for gene: FKRP were changed from to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 5; Muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation) type B, 5; Muscular dystrophy-dystroglycanopathy (limb-girdle) type C, 5
Cataract v0.36 FKRP Zornitza Stark Publications for gene: FKRP were set to
Cataract v0.35 FKRP Zornitza Stark Mode of inheritance for gene: FKRP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Cataract v0.34 FKRP Zornitza Stark Classified gene: FKRP as Amber List (moderate evidence)
Cataract v0.34 FKRP Zornitza Stark Gene: fkrp has been classified as Amber List (Moderate Evidence).
Hereditary Neuropathy - complex v0.13 AMPD2 Bryony Thompson Marked gene: AMPD2 as ready
Hereditary Neuropathy - complex v0.13 AMPD2 Bryony Thompson Gene: ampd2 has been classified as Red List (Low Evidence).
Hereditary Neuropathy - complex v0.13 AMPD2 Bryony Thompson reviewed gene: AMPD2: Rating: RED; Mode of pathogenicity: None; Publications: 27066553; Phenotypes: ; Mode of inheritance: None
Mitochondrial disease v0.319 XPNPEP3 Zornitza Stark Classified gene: XPNPEP3 as Red List (low evidence)
Mitochondrial disease v0.319 XPNPEP3 Zornitza Stark Gene: xpnpep3 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.318 XPNPEP3 Zornitza Stark reviewed gene: XPNPEP3: Rating: RED; Mode of pathogenicity: None; Publications: 20179356; Phenotypes: Nephronophthisis-like nephropathy 1, MIM#613159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary Neuropathy_CMT - isolated v0.6 RBM7 Bryony Thompson Marked gene: RBM7 as ready
Hereditary Neuropathy_CMT - isolated v0.6 RBM7 Bryony Thompson Gene: rbm7 has been classified as Amber List (Moderate Evidence).
Hereditary Neuropathy_CMT - isolated v0.6 RBM7 Bryony Thompson Classified gene: RBM7 as Amber List (moderate evidence)
Hereditary Neuropathy_CMT - isolated v0.6 RBM7 Bryony Thompson Gene: rbm7 has been classified as Amber List (Moderate Evidence).
Hereditary Neuropathy - complex v0.13 Bryony Thompson removed gene:RBM7 from the panel
Hereditary Neuropathy_CMT - isolated v0.5 RBM7 Bryony Thompson gene: RBM7 was added
gene: RBM7 was added to Hereditary Neuropathy - isolated_RMH. Sources: Expert list
Mode of inheritance for gene: RBM7 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: RBM7 were set to 27193168
Phenotypes for gene: RBM7 were set to SMA-like spinal motor neuropathy; dHMN/dSMA
Review for gene: RBM7 was set to AMBER
Added comment: Single case with a homozygote variant, with functional assays in patient fibroblasts. Also, supporting zebrafish model.
Sources: Expert list
Hereditary Neuropathy - complex v0.12 PEX10 Bryony Thompson changed review comment from: Three unrelated families/cases reported with axonal motor neuropathy; to: Three unrelated families/cases reported with a complex phenotype including axonal motor neuropathy
Hereditary Neuropathy - complex v0.12 PEX10 Bryony Thompson Marked gene: PEX10 as ready
Hereditary Neuropathy - complex v0.12 PEX10 Bryony Thompson Gene: pex10 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.12 PEX10 Bryony Thompson Classified gene: PEX10 as Green List (high evidence)
Hereditary Neuropathy - complex v0.12 PEX10 Bryony Thompson Gene: pex10 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.11 PEX10 Bryony Thompson reviewed gene: PEX10: Rating: GREEN; Mode of pathogenicity: None; Publications: 27230853, 20695019; Phenotypes: Peroxisome biogenesis disorder 6A (Zellweger) MIM#614870, Peroxisome biogenesis disorder 6B MIM#614871; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cataract v0.33 FKRP Lauren Akesson reviewed gene: FKRP: Rating: AMBER; Mode of pathogenicity: None; Publications: 30461124, 24139536, 20236121, 15833426; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 5, Muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation) type B, 5, Muscular dystrophy-dystroglycanopathy (limb-girdle) type C, 5; Mode of inheritance: None
Hereditary Neuropathy_CMT - isolated v0.4 PDK3 Bryony Thompson Marked gene: PDK3 as ready
Hereditary Neuropathy_CMT - isolated v0.4 PDK3 Bryony Thompson Gene: pdk3 has been classified as Green List (High Evidence).
Hereditary Neuropathy_CMT - isolated v0.4 PDK3 Bryony Thompson Classified gene: PDK3 as Green List (high evidence)
Hereditary Neuropathy_CMT - isolated v0.4 PDK3 Bryony Thompson Gene: pdk3 has been classified as Green List (High Evidence).
Hereditary Neuropathy_CMT - isolated v0.3 PDK3 Bryony Thompson gene: PDK3 was added
gene: PDK3 was added to Hereditary Neuropathy - isolated_RMH. Sources: Expert list
Mode of inheritance for gene: PDK3 was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Publications for gene: PDK3 were set to 23297365; 26801680; 27388934; 28902413
Phenotypes for gene: PDK3 were set to Charcot-Marie-Tooth disease, X-linked dominant, 6 MIM#300905; HMSN
Review for gene: PDK3 was set to GREEN
Added comment: Two unrelated families with the same variant and a single CMT case with another variant, and functional analyses conducted in patient fibroblasts and cell lines.
Sources: Expert list
Hereditary Neuropathy - complex v0.11 Bryony Thompson removed gene:PDK3 from the panel
Hereditary Neuropathy - complex v0.10 ASCC1 Bryony Thompson Marked gene: ASCC1 as ready
Hereditary Neuropathy - complex v0.10 ASCC1 Bryony Thompson Gene: ascc1 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.10 ASCC1 Bryony Thompson Classified gene: ASCC1 as Green List (high evidence)
Hereditary Neuropathy - complex v0.10 ASCC1 Bryony Thompson Gene: ascc1 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.9 ASCC1 Bryony Thompson edited their review of gene: ASCC1: Added comment: >3 cases/families reported with a complex neuropathy phenotype. Onset of disease is prenatal and death occurs in the first days or months of life.; Changed rating: GREEN; Changed publications: 31880396, 30327447, 26924529; Changed phenotypes: Spinal muscular atrophy with congenital bone fractures 2 MIM#616867, dHMN/dSMA; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary Neuropathy - complex v0.9 DEGS1 Bryony Thompson Marked gene: DEGS1 as ready
Hereditary Neuropathy - complex v0.9 DEGS1 Bryony Thompson Gene: degs1 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.9 DEGS1 Bryony Thompson Classified gene: DEGS1 as Green List (high evidence)
Hereditary Neuropathy - complex v0.9 DEGS1 Bryony Thompson Added comment: Comment on list classification: Complex phenotype including neuropathy
Hereditary Neuropathy - complex v0.9 DEGS1 Bryony Thompson Gene: degs1 has been classified as Green List (High Evidence).
Hereditary Neuropathy - complex v0.8 DEGS1 Bryony Thompson Deleted their review
Hereditary Neuropathy_CMT - isolated v0.1 MED25 Bryony Thompson gene: MED25 was added
gene: MED25 was added to Hereditary Neuropathy - isolated_RMH. Sources: Expert list
Mode of inheritance for gene: MED25 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MED25 were set to 19290556; 30039206
Phenotypes for gene: MED25 were set to Charcot-Marie-Tooth disease, type 2B2 MIM#605589
Review for gene: MED25 was set to RED
Added comment: Alternate cause for CMT2B2 identified in the original Costa Rican family (PMID: 19290556) in PNKP (PMID: 30039206).
Sources: Expert list
Hereditary Neuropathy - complex v0.7 DEGS1 Bryony Thompson gene: DEGS1 was added
gene: DEGS1 was added to Hereditary Neuropathy - complex_RMH. Sources: Expert list
Mode of inheritance for gene: DEGS1 was set to BIALLELIC, autosomal or pseudoautosomal
Review for gene: DEGS1 was set to GREEN
Added comment: Sources: Expert list
Hereditary Neuropathy_CMT_IsolatedAndComplex v0.1 Bryony Thompson Panel status changed from internal to public
Hereditary Neuropathy_CMT_IsolatedAndComplex v0.0 Bryony Thompson Added Panel Hereditary Neuropathy
Set child panels to: Hereditary Neuropathy - complex_RMH; Hereditary Neuropathy - isolated_RMH
Set panel types to: Royal Melbourne Hospital; Rare Disease
Mendeliome v0.1824 ZFP42 Elena Savva reviewed gene: ZFP42: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: Unknown
Mendeliome v0.1824 SLC25A21 Zornitza Stark Marked gene: SLC25A21 as ready
Mendeliome v0.1824 SLC25A21 Zornitza Stark Gene: slc25a21 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1824 SLC25A21 Zornitza Stark Classified gene: SLC25A21 as Amber List (moderate evidence)
Mendeliome v0.1824 SLC25A21 Zornitza Stark Gene: slc25a21 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1823 HTR3C Elena Savva reviewed gene: HTR3C: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 19035560, 18681779; Phenotypes: ; Mode of inheritance: Unknown
Mendeliome v0.1823 SLC25A21 Zornitza Stark gene: SLC25A21 was added
gene: SLC25A21 was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: SLC25A21 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC25A21 were set to 29517768
Phenotypes for gene: SLC25A21 were set to Mitochondrial DNA depletion syndrome-18, MIM#618811
Review for gene: SLC25A21 was set to AMBER
Added comment: One case with a homozygous variant and functional assays showing mitochondrial dysfunction.
Sources: NHS GMS
Mendeliome v0.1822 SLC25A10 Zornitza Stark Marked gene: SLC25A10 as ready
Mendeliome v0.1822 SLC25A10 Zornitza Stark Gene: slc25a10 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1822 SLC25A10 Zornitza Stark Classified gene: SLC25A10 as Amber List (moderate evidence)
Mendeliome v0.1822 SLC25A10 Zornitza Stark Gene: slc25a10 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1821 SLC25A10 Zornitza Stark gene: SLC25A10 was added
gene: SLC25A10 was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: SLC25A10 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC25A10 were set to 29211846
Phenotypes for gene: SLC25A10 were set to Intractable epileptic encephalopathy
Review for gene: SLC25A10 was set to AMBER
Added comment: One case with intractable epileptic encephalopathy with complex I deficiency, with biallelic variants. Yeast SLC25A10 ortholog lack-of-function causes impairment in mitochondrial respiration, reduced mtDNA copy number and oxidative stress vulnerability.
Sources: NHS GMS
Intellectual disability syndromic and non-syndromic v0.2476 QARS Zornitza Stark Marked gene: QARS as ready
Intellectual disability syndromic and non-syndromic v0.2476 QARS Zornitza Stark Gene: qars has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2476 QARS Zornitza Stark Phenotypes for gene: QARS were changed from to Microcephaly, progressive, seizures, and cerebral and cerebellar atrophy, MIM# 615760
Intellectual disability syndromic and non-syndromic v0.2475 QARS Zornitza Stark Publications for gene: QARS were set to
Intellectual disability syndromic and non-syndromic v0.2474 QARS Zornitza Stark Mode of inheritance for gene: QARS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2473 QARS Zornitza Stark reviewed gene: QARS: Rating: GREEN; Mode of pathogenicity: None; Publications: 28620870, 25471517, 25432320, 25041233, 24656866, 32042906; Phenotypes: Microcephaly, progressive, seizures, and cerebral and cerebellar atrophy, MIM# 615760; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genetic Epilepsy v0.638 QARS Zornitza Stark Marked gene: QARS as ready
Genetic Epilepsy v0.638 QARS Zornitza Stark Gene: qars has been classified as Green List (High Evidence).
Genetic Epilepsy v0.638 QARS Zornitza Stark Phenotypes for gene: QARS were changed from to Microcephaly, progressive, seizures, and cerebral and cerebellar atrophy, MIM# 615760
Genetic Epilepsy v0.637 QARS Zornitza Stark Publications for gene: QARS were set to
Genetic Epilepsy v0.636 QARS Zornitza Stark Mode of inheritance for gene: QARS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Genetic Epilepsy v0.635 QARS Zornitza Stark reviewed gene: QARS: Rating: GREEN; Mode of pathogenicity: None; Publications: 28620870, 25471517, 25432320, 25041233, 24656866, 32042906; Phenotypes: Microcephaly, progressive, seizures, and cerebral and cerebellar atrophy, MIM# 615760; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1820 QARS Zornitza Stark Marked gene: QARS as ready
Mendeliome v0.1820 QARS Zornitza Stark Gene: qars has been classified as Green List (High Evidence).
Mendeliome v0.1820 QARS Zornitza Stark Phenotypes for gene: QARS were changed from to Microcephaly, progressive, seizures, and cerebral and cerebellar atrophy, MIM# 615760
Mendeliome v0.1819 QARS Zornitza Stark Publications for gene: QARS were set to Encodes t-RNA synthetase, over 20 individuals reported, include in mito panel in line with other t-RNA synthetases.
Mendeliome v0.1818 QARS Zornitza Stark Publications for gene: QARS were set to
Mendeliome v0.1817 QARS Zornitza Stark Mode of inheritance for gene: QARS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1816 QARS Zornitza Stark reviewed gene: QARS: Rating: GREEN; Mode of pathogenicity: None; Publications: 28620870, 25471517, 25432320, 25041233, 24656866, 32042906; Phenotypes: Microcephaly, progressive, seizures, and cerebral and cerebellar atrophy, MIM# 615760; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.318 QARS Zornitza Stark Marked gene: QARS as ready
Mitochondrial disease v0.318 QARS Zornitza Stark Gene: qars has been classified as Green List (High Evidence).
Mitochondrial disease v0.318 QARS Zornitza Stark Classified gene: QARS as Green List (high evidence)
Mitochondrial disease v0.318 QARS Zornitza Stark Gene: qars has been classified as Green List (High Evidence).
Mitochondrial disease v0.317 QARS Zornitza Stark gene: QARS was added
gene: QARS was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: QARS was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: QARS were set to 28620870; 25471517; 25432320; 25041233; 24656866; 32042906
Phenotypes for gene: QARS were set to Microcephaly, progressive, seizures, and cerebral and cerebellar atrophy, MIM# 615760
Review for gene: QARS was set to GREEN
Added comment: Encodes t-RNA synthetase, over 20 individuals reported, include in mito panel in line with other t-RNA synthetases.
Sources: NHS GMS
Mendeliome v0.1816 PTCD3 Zornitza Stark Marked gene: PTCD3 as ready
Mendeliome v0.1816 PTCD3 Zornitza Stark Gene: ptcd3 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1816 PTCD3 Zornitza Stark Classified gene: PTCD3 as Amber List (moderate evidence)
Mendeliome v0.1816 PTCD3 Zornitza Stark Gene: ptcd3 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1815 PTCD3 Zornitza Stark gene: PTCD3 was added
gene: PTCD3 was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: PTCD3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PTCD3 were set to 30607703; 19427859
Phenotypes for gene: PTCD3 were set to Intellectual disability; optic atrophy; Leigh-like syndrome
Review for gene: PTCD3 was set to AMBER
Added comment: One compound heterozygote case and functional assays. Essential subunit of oxidative phosphorylation (OXPHOS) complexes.
Sources: NHS GMS
Mendeliome v0.1814 PTCD1 Zornitza Stark gene: PTCD1 was added
gene: PTCD1 was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: PTCD1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PTCD1 were set to 25058219
Phenotypes for gene: PTCD1 were set to Cardiomyopathy
Review for gene: PTCD1 was set to RED
Added comment: Single case reported with no functional characterisation. Biochemical analyses of heart tissue identified global COX defect. No OMIM phenotype.
Sources: NHS GMS
Mendeliome v0.1813 PNPLA4 Zornitza Stark Marked gene: PNPLA4 as ready
Mendeliome v0.1813 PNPLA4 Zornitza Stark Gene: pnpla4 has been classified as Red List (Low Evidence).
Mendeliome v0.1813 PNPLA4 Zornitza Stark Publications for gene: PNPLA4 were set to
Mendeliome v0.1812 PNPLA4 Zornitza Stark Mode of inheritance for gene: PNPLA4 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Mendeliome v0.1811 PNPLA4 Zornitza Stark Classified gene: PNPLA4 as Red List (low evidence)
Mendeliome v0.1811 PNPLA4 Zornitza Stark Gene: pnpla4 has been classified as Red List (Low Evidence).
Mendeliome v0.1810 PNPLA4 Zornitza Stark edited their review of gene: PNPLA4: Changed rating: RED
Mitochondrial disease v0.316 PNPLA4 Zornitza Stark Publications for gene: PNPLA4 were set to
Mitochondrial disease v0.315 PNPLA4 Zornitza Stark Mode of inheritance for gene: PNPLA4 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Mitochondrial disease v0.314 PNPLA4 Zornitza Stark Classified gene: PNPLA4 as Red List (low evidence)
Mitochondrial disease v0.314 PNPLA4 Zornitza Stark Gene: pnpla4 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.313 PNPLA4 Zornitza Stark edited their review of gene: PNPLA4: Changed rating: RED
Mendeliome v0.1810 OXA1L Zornitza Stark Marked gene: OXA1L as ready
Mendeliome v0.1810 OXA1L Zornitza Stark Gene: oxa1l has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1810 OXA1L Zornitza Stark Classified gene: OXA1L as Amber List (moderate evidence)
Mendeliome v0.1810 OXA1L Zornitza Stark Gene: oxa1l has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1809 OXA1L Zornitza Stark gene: OXA1L was added
gene: OXA1L was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: OXA1L was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: OXA1L were set to 30201738; 16435202
Phenotypes for gene: OXA1L were set to Encephalopathy; hypotonia; developmental delay
Review for gene: OXA1L was set to AMBER
Added comment: Single family reported with biochemical and molecular analyses of patient skeletal muscle and fibroblasts. In vitro functional assays in human cell lines, Drosophila model, and yeast-based assays. Loss of function affects oxidative phosphorylation complexes IV and V.
Sources: NHS GMS
Mendeliome v0.1808 NSUN3 Zornitza Stark Marked gene: NSUN3 as ready
Mendeliome v0.1808 NSUN3 Zornitza Stark Gene: nsun3 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1808 NSUN3 Zornitza Stark Classified gene: NSUN3 as Amber List (moderate evidence)
Mendeliome v0.1808 NSUN3 Zornitza Stark Gene: nsun3 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1807 NSUN3 Zornitza Stark gene: NSUN3 was added
gene: NSUN3 was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: NSUN3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NSUN3 were set to 27356879
Phenotypes for gene: NSUN3 were set to combined mitochondrial respiratory chain complex deficiency
Review for gene: NSUN3 was set to AMBER
Added comment: A single compound heterozygous case. Patient-derived fibroblasts exhibited severe defects in mitochondrial translation that can be rescued by exogenous expression of NSun3. In vitro functional assays also conducted.
Sources: NHS GMS
Mitochondrial disease v0.313 CISD2 Bryony Thompson gene: CISD2 was added
gene: CISD2 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: CISD2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CISD2 were set to 29237418; 28335035; 27459537; 26230298; 17846994
Phenotypes for gene: CISD2 were set to Wolfram syndrome 2 MIM#604928
Review for gene: CISD2 was set to GREEN
Added comment: At least 3 families and a mouse model. Culture of patient-derived fibroblasts in glucose-free galactose medium revealed a respiratory chain defect in complexes I and II, and a trend towards decreased ATP levels.
Sources: NHS GMS
Cataract v0.33 EPCAM Lauren Akesson reviewed gene: EPCAM: Rating: RED; Mode of pathogenicity: None; Publications: 30461124; Phenotypes: Congenital diarrhoea 5 with tufting enteropathy, Lynch syndrome; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cataract v0.33 EED Lauren Akesson gene: EED was added
gene: EED was added to Cataract. Sources: Literature
Mode of inheritance for gene: EED was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: EED were set to 25787343
Phenotypes for gene: EED were set to Cohen-Gibson syndrome
Penetrance for gene: EED were set to unknown
Review for gene: EED was set to AMBER
Added comment: Cataract has been reported in a single proband with a heterozygous missense variant in EED (no functional studies performed) (PMID 25787343). Cataracts have not been reported in subsequent probands (PMID 27193220 ; 27868325 ; 28229514 ; 29410511 ; 30858506).
Sources: Literature
Mitochondrial disease v0.312 COX4I1 Bryony Thompson gene: COX4I1 was added
gene: COX4I1 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: COX4I1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: COX4I1 were set to 28766551
Phenotypes for gene: COX4I1 were set to short stature; mild dysmorphic features; Fanconi anemia
Review for gene: COX4I1 was set to RED
Added comment: Single family with a homozygous variant, with assays in patient fibroblasts only.
Sources: NHS GMS
Mitochondrial disease v0.311 NNT Zornitza Stark Marked gene: NNT as ready
Mitochondrial disease v0.311 NNT Zornitza Stark Gene: nnt has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.311 NNT Zornitza Stark Classified gene: NNT as Amber List (moderate evidence)
Mitochondrial disease v0.311 NNT Zornitza Stark Gene: nnt has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.310 NNT Zornitza Stark reviewed gene: NNT: Rating: AMBER; Mode of pathogenicity: None; Publications: 25778941; Phenotypes: Glucocorticoid deficiency 4, with or without mineralocorticoid deficiency MIM#614736; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.310 COX5A Bryony Thompson gene: COX5A was added
gene: COX5A was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: COX5A was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: COX5A were set to 28247525
Phenotypes for gene: COX5A were set to pulmonary arterial hypertension; lactic acidemia; failure to thrive; isolated complex IV deficiency
Review for gene: COX5A was set to RED
Added comment: Single family with a homozygous variant, with assays conducted in patient fibroblasts only.
Sources: NHS GMS
Mendeliome v0.1806 NDUFB10 Zornitza Stark Marked gene: NDUFB10 as ready
Mendeliome v0.1806 NDUFB10 Zornitza Stark Gene: ndufb10 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1806 NDUFB10 Zornitza Stark Classified gene: NDUFB10 as Amber List (moderate evidence)
Mendeliome v0.1806 NDUFB10 Zornitza Stark Gene: ndufb10 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1805 NDUFB10 Zornitza Stark gene: NDUFB10 was added
gene: NDUFB10 was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: NDUFB10 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NDUFB10 were set to 28040730; 32025618
Phenotypes for gene: NDUFB10 were set to fatal infantile lactic acidosis; cardiomyopathy
Review for gene: NDUFB10 was set to AMBER
Added comment: Single compound heterozygote case and mitochondrial phenotype. Assays of respiratory chain enzyme activities and functions in patient tissues/fibroblasts and in vitro functional assays. Plant model system supporting mitochondrial complex I dysfunction.
Sources: NHS GMS
Cataract v0.33 DOCK8 Lauren Akesson reviewed gene: DOCK8: Rating: RED; Mode of pathogenicity: None; Publications: 18060736; Phenotypes: Hyper-IgE recurrent infection syndrome 243700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cataract v0.33 DCLRE1C Lauren Akesson reviewed gene: DCLRE1C: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Omenn syndrome 603554, Severe combined immunodeficiency, Athabascan type 602450; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cataract v0.33 CYBB Lauren Akesson reviewed gene: CYBB: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Chronic granulomatous disease, immunodeficiency 34 with mycobacteriosis; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Cataract v0.33 CYBA Lauren Akesson reviewed gene: CYBA: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Chronic granulomatous disease; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.309 KIF5A Bryony Thompson gene: KIF5A was added
gene: KIF5A was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: KIF5A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: KIF5A were set to 27463701; 27414745
Phenotypes for gene: KIF5A were set to Myoclonus, intractable, neonatal MIM#617235
Mode of pathogenicity for gene: KIF5A was set to Other
Review for gene: KIF5A was set to AMBER
Added comment: Three unrelated cases with de novo heterozygous predicted stop-loss variants with read-through of the normal termination codon to create an elongated protein and predicted to be dominant-negative. One of the cases was diagnosed with complex IV deficiency based on a high suspicion of mitochondrial disease given the clinical presentation and borderline findings on electron transport chain studies. There is no evidence that heterozygous variants associated with spastic paraplegia are linked to mitochondrial dysfunction.
Sources: NHS GMS
Mitochondrial disease v0.308 MICU2 Bryony Thompson Marked gene: MICU2 as ready
Mitochondrial disease v0.308 MICU2 Bryony Thompson Gene: micu2 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.308 MICU2 Bryony Thompson gene: MICU2 was added
gene: MICU2 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: MICU2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MICU2 were set to 29053821
Phenotypes for gene: MICU2 were set to cognitive impairment; spasticity; white matter involvement
Review for gene: MICU2 was set to RED
Added comment: Single multiplex consanguineous family segregating a homozygous truncating variant. Abnormal mitochondrial calcium homeostasis in patient cells.
Sources: NHS GMS
Mitochondrial disease v0.307 NAXD Bryony Thompson Marked gene: NAXD as ready
Mitochondrial disease v0.307 NAXD Bryony Thompson Gene: naxd has been classified as Green List (High Evidence).
Mitochondrial disease v0.307 NAXD Bryony Thompson Classified gene: NAXD as Green List (high evidence)
Mitochondrial disease v0.307 NAXD Bryony Thompson Gene: naxd has been classified as Green List (High Evidence).
Mitochondrial disease v0.306 NAXD Bryony Thompson gene: NAXD was added
gene: NAXD was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: NAXD was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NAXD were set to 30576410
Phenotypes for gene: NAXD were set to Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2 MIM#618321
Review for gene: NAXD was set to GREEN
Added comment: Six unrelated cases. Patient cells and muscle biopsies also showed impaired mitochondrial function, higher sensitivity to metabolic stress, and decreased mitochondrial reactive oxygen species production. In vitro functional assays also conducted.
Sources: NHS GMS
Mitochondrial disease v0.305 NDUFAF7 Bryony Thompson Marked gene: NDUFAF7 as ready
Mitochondrial disease v0.305 NDUFAF7 Bryony Thompson Gene: ndufaf7 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.305 NDUFAF7 Bryony Thompson gene: NDUFAF7 was added
gene: NDUFAF7 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: NDUFAF7 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: NDUFAF7 were set to 28837730
Phenotypes for gene: NDUFAF7 were set to Pathologic myopia
Review for gene: NDUFAF7 was set to RED
Added comment: Single family with heterozygous variant. In vitro functional assays conducted are not compelling evidence.
Sources: NHS GMS
Mitochondrial disease v0.304 NDUFB10 Bryony Thompson Marked gene: NDUFB10 as ready
Mitochondrial disease v0.304 NDUFB10 Bryony Thompson Gene: ndufb10 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.304 NDUFB10 Bryony Thompson Classified gene: NDUFB10 as Amber List (moderate evidence)
Mitochondrial disease v0.304 NDUFB10 Bryony Thompson Gene: ndufb10 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.303 NDUFB10 Bryony Thompson gene: NDUFB10 was added
gene: NDUFB10 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: NDUFB10 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NDUFB10 were set to 28040730; 32025618
Phenotypes for gene: NDUFB10 were set to fatal infantile lactic acidosis; cardiomyopathy
Review for gene: NDUFB10 was set to AMBER
Added comment: Single compound heterozygote case and assays of respiratory chain enzyme activities and functions in patient tissues/fibroblasts and in vitro functional assays. Plant model system supporting mitochondrial complex I dysfunction. No omim phenotype.
Sources: NHS GMS
Mitochondrial disease v0.302 NNT Bryony Thompson Classified gene: NNT as Green List (high evidence)
Mitochondrial disease v0.302 NNT Bryony Thompson Gene: nnt has been classified as Green List (High Evidence).
Mitochondrial disease v0.301 NNT Bryony Thompson gene: NNT was added
gene: NNT was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: NNT was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NNT were set to 26309815; 22634753
Phenotypes for gene: NNT were set to Glucocorticoid deficiency 4, with or without mineralocorticoid deficiency MIM#614736
Review for gene: NNT was set to GREEN
Added comment: >3 cases reported and a mouse model. A protein of the inner mitochondrial membrane with a key role in mitochondrial redox balance.
Sources: NHS GMS
Mitochondrial disease v0.300 NSUN3 Bryony Thompson Classified gene: NSUN3 as Amber List (moderate evidence)
Mitochondrial disease v0.300 NSUN3 Bryony Thompson Gene: nsun3 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.299 NSUN3 Bryony Thompson gene: NSUN3 was added
gene: NSUN3 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: NSUN3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NSUN3 were set to 27356879
Phenotypes for gene: NSUN3 were set to combined mitochondrial respiratory chain complex deficiency
Review for gene: NSUN3 was set to AMBER
Added comment: A single compound heterozygous case. Patient-derived fibroblasts exhibited severe defects in mitochondrial translation that can be rescued by exogenous expression of NSun3. In vitro functional assays also conducted.
Sources: NHS GMS
Mitochondrial disease v0.298 OXA1L Bryony Thompson Classified gene: OXA1L as Amber List (moderate evidence)
Mitochondrial disease v0.298 OXA1L Bryony Thompson Gene: oxa1l has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.297 OXA1L Bryony Thompson changed review comment from: Single family reported with biochemical and molecular analyses of patient skeletal muscle and fibroblasts. In vitro functional assays in human cell lines and a Drosophila model. Loss of function affects oxidative phosphorylation complexes IV and V.
Sources: NHS GMS; to: Single family reported with biochemical and molecular analyses of patient skeletal muscle and fibroblasts. In vitro functional assays in human cell lines, Drosophila model, and yeast-based assays. Loss of function affects oxidative phosphorylation complexes IV and V.
Sources: NHS GMS
Mitochondrial disease v0.297 OXA1L Bryony Thompson edited their review of gene: OXA1L: Changed publications: 30201738, 16435202
Mitochondrial disease v0.297 OXA1L Bryony Thompson gene: OXA1L was added
gene: OXA1L was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: OXA1L was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: OXA1L were set to 30201738
Phenotypes for gene: OXA1L were set to encephalopathy; hypotonia; developmental delay
Review for gene: OXA1L was set to AMBER
Added comment: Single family reported with biochemical and molecular analyses of patient skeletal muscle and fibroblasts. In vitro functional assays in human cell lines and a Drosophila model. Loss of function affects oxidative phosphorylation complexes IV and V.
Sources: NHS GMS
Mitochondrial disease v0.296 PET117 Bryony Thompson gene: PET117 was added
gene: PET117 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: PET117 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PET117 were set to 28386624
Phenotypes for gene: PET117 were set to Developmental delay
Review for gene: PET117 was set to RED
Added comment: Two siblings with deficiency of complex IV of the respiratory chain and a homozygous variant. Only functional assays conducted were complementation assays in patient fibroblasts.
Sources: NHS GMS
Mitochondrial disease v0.295 PITRM1 Bryony Thompson Classified gene: PITRM1 as Green List (high evidence)
Mitochondrial disease v0.295 PITRM1 Bryony Thompson Gene: pitrm1 has been classified as Green List (High Evidence).
Ataxia - paediatric v0.51 PITRM1 Bryony Thompson Marked gene: PITRM1 as ready
Ataxia - paediatric v0.51 PITRM1 Bryony Thompson Gene: pitrm1 has been classified as Green List (High Evidence).
Ataxia - paediatric v0.51 PITRM1 Bryony Thompson Classified gene: PITRM1 as Green List (high evidence)
Ataxia - paediatric v0.51 PITRM1 Bryony Thompson Gene: pitrm1 has been classified as Green List (High Evidence).
Ataxia - paediatric v0.50 PITRM1 Bryony Thompson gene: PITRM1 was added
gene: PITRM1 was added to Ataxia - paediatric. Sources: Literature
Mode of inheritance for gene: PITRM1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PITRM1 were set to 26697887; 29764912
Phenotypes for gene: PITRM1 were set to Cerebellar atrophy; mental retardation; spinocerebellar ataxia; cognitive decline; psychosis
Review for gene: PITRM1 was set to GREEN
Added comment: Three families with two unique variants and in vitro functional assays. Cases and mouse model have spinocerebellar ataxia as a prominent feature of the phenotype. No OMIM phenotype.
Sources: Literature
Mitochondrial disease v0.294 PITRM1 Bryony Thompson edited their review of gene: PITRM1: Changed rating: GREEN
Mitochondrial disease v0.294 PITRM1 Bryony Thompson gene: PITRM1 was added
gene: PITRM1 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: PITRM1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PITRM1 were set to 26697887; 29764912
Phenotypes for gene: PITRM1 were set to Cerebellar atrophy; mental retardation; spinocerebellar ataxia; cognitive decline; psychosis
Added comment: Three families with two unique variants. Mitochondrial dysfunction identified in in vitro functional assays and mouse model. No OMIM phenotype.
Sources: NHS GMS
Mitochondrial disease v0.293 PLA2G6 Bryony Thompson Marked gene: PLA2G6 as ready
Mitochondrial disease v0.293 PLA2G6 Bryony Thompson Gene: pla2g6 has been classified as Green List (High Evidence).
Mitochondrial disease v0.293 PLA2G6 Bryony Thompson Classified gene: PLA2G6 as Green List (high evidence)
Mitochondrial disease v0.293 PLA2G6 Bryony Thompson Gene: pla2g6 has been classified as Green List (High Evidence).
Mitochondrial disease v0.292 PLA2G6 Bryony Thompson gene: PLA2G6 was added
gene: PLA2G6 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: PLA2G6 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PLA2G6 were set to 25348461; 26001724; 26506412; 30528460; 16783378
Phenotypes for gene: PLA2G6 were set to Infantile neuroaxonal dystrophy 1 MIM#256600; Neurodegeneration with brain iron accumulation 2B MIM#610217; Parkinson disease 14, autosomal recessive MIM#612953
Review for gene: PLA2G6 was set to GREEN
Added comment: Findings in a Drosophila/mouse models and patient fibroblasts demonstrated that loss of normal PLA2G6 gene activity leads to lipid peroxidation, mitochondrial dysfunction and subsequent mitochondrial membrane abnormalities. >3 cases reported.
Sources: NHS GMS
Mitochondrial disease v0.291 PTCD1 Bryony Thompson changed review comment from: Single case reported with no functional characterisation. Biochemical analyses of heart tissue identified global COX defect.
Sources: NHS GMS; to: Single case reported with no functional characterisation. Biochemical analyses of heart tissue identified global COX defect. No OMIM phenotype.
Sources: NHS GMS
Mitochondrial disease v0.291 PTCD1 Bryony Thompson gene: PTCD1 was added
gene: PTCD1 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: PTCD1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PTCD1 were set to 25058219
Phenotypes for gene: PTCD1 were set to Cardiomyopathy
Review for gene: PTCD1 was set to RED
Added comment: Single case reported with no functional characterisation. Biochemical analyses of heart tissue identified global COX defect.
Sources: NHS GMS
Mitochondrial disease v0.290 PTCD3 Bryony Thompson Classified gene: PTCD3 as Amber List (moderate evidence)
Mitochondrial disease v0.290 PTCD3 Bryony Thompson Gene: ptcd3 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.289 PTCD3 Bryony Thompson gene: PTCD3 was added
gene: PTCD3 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: PTCD3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PTCD3 were set to 30607703; 19427859
Phenotypes for gene: PTCD3 were set to Mental retardation; optic atrophy; Leigh-like syndrome
Review for gene: PTCD3 was set to AMBER
Added comment: One compound heterozygote case and functional assays. Essential subunit of oxidative phosphorylation (OXPHOS) complexes.
Sources: NHS GMS
Mitochondrial disease v0.288 D2HGDH Bryony Thompson Marked gene: D2HGDH as ready
Mitochondrial disease v0.288 D2HGDH Bryony Thompson Gene: d2hgdh has been classified as Green List (High Evidence).
Mitochondrial disease v0.288 D2HGDH Bryony Thompson Classified gene: D2HGDH as Green List (high evidence)
Mitochondrial disease v0.288 D2HGDH Bryony Thompson Gene: d2hgdh has been classified as Green List (High Evidence).
Mitochondrial disease v0.287 D2HGDH Bryony Thompson gene: D2HGDH was added
gene: D2HGDH was added to Mitochondrial disease. Sources: Literature,NHS GMS
Mode of inheritance for gene: D2HGDH was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: D2HGDH were set to 25778941; 31349060; 15609246; 20020533
Phenotypes for gene: D2HGDH were set to D-2-hydroxyglutaric aciduria MIM#600721
Review for gene: D2HGDH was set to GREEN
Added comment: Enzyme catalyses oxidation of D-2HG, which is coupled to the mitochondrial electron transport chain. >3 cases reported.
Sources: Literature, NHS GMS
Mitochondrial disease v0.286 IDH2 Bryony Thompson Marked gene: IDH2 as ready
Mitochondrial disease v0.286 IDH2 Bryony Thompson Gene: idh2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.286 IDH2 Bryony Thompson Classified gene: IDH2 as Green List (high evidence)
Mitochondrial disease v0.286 IDH2 Bryony Thompson Gene: idh2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.285 IDH2 Bryony Thompson gene: IDH2 was added
gene: IDH2 was added to Mitochondrial disease. Sources: Literature
Mode of inheritance for gene: IDH2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: IDH2 were set to 25778941; 27142242; 20847235; 24049096
Phenotypes for gene: IDH2 were set to D-2-hydroxyglutaric aciduria 2 MIM#613657
Review for gene: IDH2 was set to GREEN
Added comment: Loss of IDH2 induces mitochondrial dysfunction in a mouse model. 17 cases with a de novo or inherited from a mosaic carrier (R140G, R140Q) have been reported.
Sources: Literature
Mitochondrial disease v0.284 PANK2 Bryony Thompson Marked gene: PANK2 as ready
Mitochondrial disease v0.284 PANK2 Bryony Thompson Gene: pank2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.284 PANK2 Bryony Thompson Classified gene: PANK2 as Green List (high evidence)
Mitochondrial disease v0.284 PANK2 Bryony Thompson Gene: pank2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.283 PANK2 Bryony Thompson gene: PANK2 was added
gene: PANK2 was added to Mitochondrial disease. Sources: Literature,NHS GMS
Mode of inheritance for gene: PANK2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PANK2 were set to 25778941; 11479594; 12510040; 28863176
Phenotypes for gene: PANK2 were set to HARP syndrome MIM#607236; Neurodegeneration with brain iron accumulation 1 MIM#234200
Review for gene: PANK2 was set to GREEN
Added comment: A mitochondrial enzyme, which phosphorylates vitamin B5 in the first reaction of the CoA biosynthetic pathway (a relevant mitochondrial cofactor). >3 cases reported.
Sources: Literature, NHS GMS
Mitochondrial disease v0.282 COASY Bryony Thompson Marked gene: COASY as ready
Mitochondrial disease v0.282 COASY Bryony Thompson Gene: coasy has been classified as Green List (High Evidence).
Mitochondrial disease v0.282 COASY Bryony Thompson Classified gene: COASY as Green List (high evidence)
Mitochondrial disease v0.282 COASY Bryony Thompson Gene: coasy has been classified as Green List (High Evidence).
Mitochondrial disease v0.281 COASY Bryony Thompson gene: COASY was added
gene: COASY was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: COASY was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: COASY were set to 25778941; 24360804; 30089828; 28489334
Phenotypes for gene: COASY were set to Neurodegeneration with brain iron accumulation 6 MIM#615643; Pontocerebellar hypoplasia, type 12 MIM#618266
Review for gene: COASY was set to GREEN
Added comment: A bi-functional mitochondrial enzyme, which catalyzes the final steps of CoA biosynthesis, a relevant mitochondrial cofactor. >3 cases reported.
Sources: NHS GMS, Literature
Mitochondrial disease v0.280 PPOX Bryony Thompson Marked gene: PPOX as ready
Mitochondrial disease v0.280 PPOX Bryony Thompson Gene: ppox has been classified as Green List (High Evidence).
Mitochondrial disease v0.280 PPOX Bryony Thompson Classified gene: PPOX as Green List (high evidence)
Mitochondrial disease v0.280 PPOX Bryony Thompson Gene: ppox has been classified as Green List (High Evidence).
Mitochondrial disease v0.279 PPOX Bryony Thompson gene: PPOX was added
gene: PPOX was added to Mitochondrial disease. Sources: Literature,NHS GMS
Mode of inheritance for gene: PPOX was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: PPOX were set to 25778941; 9811936; 12859407; 30476629
Phenotypes for gene: PPOX were set to Porphyria variegata MIM#176200
Review for gene: PPOX was set to GREEN
Added comment: Variegate porphyria is a disorder of heme metabolism resulting from a deficiency in protoporphyrinogen oxidase, an enzyme located on the inner mitochondrial membrane. A defect in a relevant mitochondrial cofactor. >3 cases reported.
Sources: Literature, NHS GMS
Mitochondrial disease v0.278 HADHB Bryony Thompson Marked gene: HADHB as ready
Mitochondrial disease v0.278 HADHB Bryony Thompson Gene: hadhb has been classified as Green List (High Evidence).
Mitochondrial disease v0.278 HADHB Bryony Thompson Classified gene: HADHB as Green List (high evidence)
Mitochondrial disease v0.278 HADHB Bryony Thompson Gene: hadhb has been classified as Green List (High Evidence).
Mitochondrial disease v0.277 HADHB Bryony Thompson gene: HADHB was added
gene: HADHB was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: HADHB was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: HADHB were set to 25778941; 30682426; 9259266; 29956646
Phenotypes for gene: HADHB were set to Trifunctional protein deficiency MIM#609015
Review for gene: HADHB was set to GREEN
Added comment: The heterooctameric mitochondrial trifunctional protein (MTP), composed of four α- and β-subunits harbours three enzymes that each perform a different function in mitochondrial fatty acid β-oxidation. MTP deficiency is a defect in the substrate-generating upstream reactions of OXPHOS. >3 cases reported.
Sources: NHS GMS, Literature
Mitochondrial disease v0.276 HADHA Bryony Thompson Marked gene: HADHA as ready
Mitochondrial disease v0.276 HADHA Bryony Thompson Gene: hadha has been classified as Green List (High Evidence).
Mitochondrial disease v0.276 HADHA Bryony Thompson Classified gene: HADHA as Green List (high evidence)
Mitochondrial disease v0.276 HADHA Bryony Thompson Gene: hadha has been classified as Green List (High Evidence).
Mitochondrial disease v0.275 HADHA Bryony Thompson gene: HADHA was added
gene: HADHA was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: HADHA was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: HADHA were set to 25778941; 7811722; 29459657
Phenotypes for gene: HADHA were set to LCHAD deficiency MIM#609016; Trifunctional protein deficiency MIM#609015
Review for gene: HADHA was set to GREEN
Added comment: Long-Chain-3-Hydroxy-Acyl-CoA-Dehydrogenase-Deficiency (LCHADD) is an inherited disorder affecting mitochondrial fatty acid β-oxidation. A defect in the substrate-generating upstream reactions of OXPHOS. >3 cases reported. Also affects mitochondrial morphology.
Sources: NHS GMS, Literature
Mendeliome v0.1804 NDUFA4 Zornitza Stark Classified gene: NDUFA4 as Green List (high evidence)
Mendeliome v0.1804 NDUFA4 Zornitza Stark Gene: ndufa4 has been classified as Green List (High Evidence).
Mendeliome v0.1803 NDUFA4 Zornitza Stark changed review comment from: Single family and a lot of functional data. Encodes a complex IV subunit.; to: Single family and a lot of functional data. Unpublished data on another family. Encodes a complex IV subunit.
Mendeliome v0.1803 NDUFA4 Zornitza Stark edited their review of gene: NDUFA4: Changed rating: GREEN
Mitochondrial disease v0.274 NDUFA4 Zornitza Stark Classified gene: NDUFA4 as Green List (high evidence)
Mitochondrial disease v0.274 NDUFA4 Zornitza Stark Gene: ndufa4 has been classified as Green List (High Evidence).
Mitochondrial disease v0.273 NDUFA4 Zornitza Stark changed review comment from: Single family and a lot of functional data. Encodes a complex IV subunit.; to: Single family and a lot of functional data. Unpublished data on another family. Encodes a complex IV subunit.
Mitochondrial disease v0.273 NDUFA4 Zornitza Stark edited their review of gene: NDUFA4: Changed rating: GREEN
Mendeliome v0.1803 MRPS14 Zornitza Stark Marked gene: MRPS14 as ready
Mendeliome v0.1803 MRPS14 Zornitza Stark Gene: mrps14 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1803 MRPS14 Zornitza Stark Classified gene: MRPS14 as Amber List (moderate evidence)
Mendeliome v0.1803 MRPS14 Zornitza Stark Gene: mrps14 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1802 MRPS14 Zornitza Stark edited their review of gene: MRPS14: Changed rating: AMBER; Changed phenotypes: Combined oxidative phosphorylation deficiency 38, MIM# 618378
Mitochondrial disease v0.273 MRPS14 Zornitza Stark Classified gene: MRPS14 as Amber List (moderate evidence)
Mitochondrial disease v0.273 MRPS14 Zornitza Stark Gene: mrps14 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.272 MRPS14 Zornitza Stark edited their review of gene: MRPS14: Changed rating: AMBER; Changed phenotypes: Combined oxidative phosphorylation deficiency 38, MIM# 618378
Mitochondrial disease v0.272 HADH Bryony Thompson Marked gene: HADH as ready
Mitochondrial disease v0.272 HADH Bryony Thompson Gene: hadh has been classified as Green List (High Evidence).
Mitochondrial disease v0.272 HADH Bryony Thompson Classified gene: HADH as Green List (high evidence)
Mitochondrial disease v0.272 HADH Bryony Thompson Gene: hadh has been classified as Green List (High Evidence).
Mitochondrial disease v0.271 HADH Bryony Thompson Classified gene: HADH as Amber List (moderate evidence)
Mitochondrial disease v0.271 HADH Bryony Thompson Gene: hadh has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.270 HADH Bryony Thompson gene: HADH was added
gene: HADH was added to Mitochondrial disease. Sources: Literature,NHS GMS
Mode of inheritance for gene: HADH was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: HADH were set to 25778941; 23430856; 27771675; 11489939
Phenotypes for gene: HADH were set to 3-hydroxyacyl-CoA dehydrogenase deficiency MIM#231530
Review for gene: HADH was set to GREEN
Added comment: Short-chain-L-3-hydroxyacyl-CoA dehydrogenase deficiency is an inherited disorder affecting mitochondrial fatty acid β-oxidation. A defect in the substrate-generating upstream reactions of OXPHOS. >3 cases reported.
Sources: Literature, NHS GMS
Mitochondrial disease v0.269 CPT2 Bryony Thompson Mode of inheritance for gene: CPT2 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mitochondrial disease v0.268 CPT2 Bryony Thompson edited their review of gene: CPT2: Changed phenotypes: CPT II deficiency, infantile MIM#600649, CPT II deficiency, lethal neonatal MIM#608836, CPT II deficiency, myopathic, stress-induced MIM#255110; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mitochondrial disease v0.268 CPT2 Bryony Thompson Marked gene: CPT2 as ready
Mitochondrial disease v0.268 CPT2 Bryony Thompson Gene: cpt2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.268 CPT2 Bryony Thompson Classified gene: CPT2 as Green List (high evidence)
Mitochondrial disease v0.268 CPT2 Bryony Thompson Gene: cpt2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.267 CPT2 Bryony Thompson gene: CPT2 was added
gene: CPT2 was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: CPT2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CPT2 were set to 25778941; 12673791; 30957255
Phenotypes for gene: CPT2 were set to CPT II deficiency, infantile MIM#600649; CPT II deficiency, lethal neonatal MIM#608836; CPT II deficiency, myopathic, stress-induced MIM#255110
Review for gene: CPT2 was set to GREEN
Added comment: Carnitine palmitoyltransferase II (CPT2) is a rare autosomal recessive inherited disorder affecting mitochondrial fatty acid β-oxidation. A defect in the substrate-generating upstream reactions of OXPHOS. >3 cases reported.
Sources: NHS GMS, Literature
Mitochondrial disease v0.266 CPT1A Bryony Thompson Marked gene: CPT1A as ready
Mitochondrial disease v0.266 CPT1A Bryony Thompson Gene: cpt1a has been classified as Green List (High Evidence).
Mitochondrial disease v0.266 CPT1A Bryony Thompson Classified gene: CPT1A as Green List (high evidence)
Mitochondrial disease v0.266 CPT1A Bryony Thompson Gene: cpt1a has been classified as Green List (High Evidence).
Mitochondrial disease v0.265 CPT1A Bryony Thompson gene: CPT1A was added
gene: CPT1A was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: CPT1A was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CPT1A were set to 25778941; 12189492; 23430932
Phenotypes for gene: CPT1A were set to CPT deficiency, hepatic, type IA MIM#255120
Review for gene: CPT1A was set to GREEN
Added comment: Hepatic carnitine palmitoyltransferase (CPT) deficiency type 1A is a disorder of mitochondrial fatty acid oxidation. A defect in the substrate-generating upstream reactions of OXPHOS. >3 cases reported.
Sources: NHS GMS, Literature
Mendeliome v0.1802 MRM2 Zornitza Stark Marked gene: MRM2 as ready
Mendeliome v0.1802 MRM2 Zornitza Stark Gene: mrm2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1802 MRM2 Zornitza Stark Classified gene: MRM2 as Amber List (moderate evidence)
Mendeliome v0.1802 MRM2 Zornitza Stark Gene: mrm2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1801 MRM2 Zornitza Stark gene: MRM2 was added
gene: MRM2 was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: MRM2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MRM2 were set to 28973171
Phenotypes for gene: MRM2 were set to MELAS-like
Review for gene: MRM2 was set to AMBER
Added comment: Single individual reported plus functional data. MRM2 encodes an enzyme responsible for 2'-O-methyl modification at position U1369 in the human mitochondrial 16S rRNA.
Sources: NHS GMS
Intellectual disability syndromic and non-syndromic v0.2473 MRPL3 Zornitza Stark reviewed gene: MRPL3: Rating: AMBER; Mode of pathogenicity: None; Publications: 27815843, 21786366; Phenotypes: Combined oxidative phosphorylation deficiency 9, OMIM #614582; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.264 ACADVL Bryony Thompson Marked gene: ACADVL as ready
Mitochondrial disease v0.264 ACADVL Bryony Thompson Gene: acadvl has been classified as Green List (High Evidence).
Mitochondrial disease v0.264 ACADVL Bryony Thompson Classified gene: ACADVL as Green List (high evidence)
Mitochondrial disease v0.264 ACADVL Bryony Thompson Gene: acadvl has been classified as Green List (High Evidence).
Mitochondrial disease v0.263 ACADVL Bryony Thompson gene: ACADVL was added
gene: ACADVL was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: ACADVL was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ACADVL were set to 25778941; 8845838; 29459657
Phenotypes for gene: ACADVL were set to VLCAD deficiency MIM#201475
Review for gene: ACADVL was set to GREEN
Added comment: Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a mitochondrial fatty acid oxidation disorder. A defect in the substrate-generating upstream reactions of OXPHOS. >3 cases reported.
Sources: NHS GMS, Literature
Mitochondrial disease v0.262 MRPL3 Zornitza Stark Classified gene: MRPL3 as Green List (high evidence)
Mitochondrial disease v0.262 MRPL3 Zornitza Stark Gene: mrpl3 has been classified as Green List (High Evidence).
Mendeliome v0.1800 MRPL3 Zornitza Stark Classified gene: MRPL3 as Green List (high evidence)
Mendeliome v0.1800 MRPL3 Zornitza Stark Gene: mrpl3 has been classified as Green List (High Evidence).
Mendeliome v0.1799 MRPL3 Zornitza Stark changed review comment from: 1 French family with 4 sibs with severe mitochondrial disorder - compound heterozygous mutations in the MRPL3 gene, no functional studies. 1 male infant with a severe mitochondrial disorder - compound heterozygous mutations in the MRPL3 gene, no functional studies.; to: 1 French family with 4 sibs with severe mitochondrial disorder - compound heterozygous mutations in the MRPL3 gene, some functional studies. 1 male infant with a severe mitochondrial disorder - compound heterozygous mutations in the MRPL3 gene, no functional studies.
Mendeliome v0.1799 MRPL3 Zornitza Stark edited their review of gene: MRPL3: Changed rating: GREEN
Mitochondrial disease v0.261 MRPL3 Zornitza Stark edited their review of gene: MRPL3: Changed rating: GREEN
Mitochondrial disease v0.261 MRPL3 Zornitza Stark changed review comment from: 1 French family with 4 sibs with severe mitochondrial disorder - compound heterozygous mutations in the MRPL3 gene, no functional studies. 1 male infant with a severe mitochondrial disorder - compound heterozygous mutations in the MRPL3 gene, no functional studies.; to: 1 French family with 4 sibs with severe mitochondrial disorder - compound heterozygous mutations in the MRPL3 gene, some functional studies. 1 male infant with a severe mitochondrial disorder - compound heterozygous mutations in the MRPL3 gene, no functional studies.
Mitochondrial disease v0.261 MRM2 Zornitza Stark Marked gene: MRM2 as ready
Mitochondrial disease v0.261 MRM2 Zornitza Stark Gene: mrm2 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.261 MRM2 Zornitza Stark Classified gene: MRM2 as Amber List (moderate evidence)
Mitochondrial disease v0.261 MRM2 Zornitza Stark Gene: mrm2 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.260 MRM2 Zornitza Stark gene: MRM2 was added
gene: MRM2 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: MRM2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MRM2 were set to 28973171
Phenotypes for gene: MRM2 were set to MELAS-like
Review for gene: MRM2 was set to AMBER
Added comment: Single individual reported plus functional data. MRM2 encodes an enzyme responsible for 2'-O-methyl modification at position U1369 in the human mitochondrial 16S rRNA.
Sources: NHS GMS
Mitochondrial disease v0.259 ACADSB Bryony Thompson Classified gene: ACADSB as Green List (high evidence)
Mitochondrial disease v0.259 ACADSB Bryony Thompson Gene: acadsb has been classified as Green List (High Evidence).
Mitochondrial disease v0.258 ACADSB Bryony Thompson gene: ACADSB was added
gene: ACADSB was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: ACADSB was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ACADSB were set to 25778941; 17945527
Phenotypes for gene: ACADSB were set to 2-methylbutyrylglycinuria MIM#610006
Review for gene: ACADSB was set to GREEN
Added comment: 2-Methylbutyryl-CoA dehydrogenase (MBD) deficiency is an autosomal recessive metabolic disorder of impaired isoleucine degradation, a mitochondrial disorder of fatty acid β-oxidation. A defect in the substrate-generating upstream reactions of OXPHOS. >3 cases reported. Cases are usually asymptomatic, but can have neurological symptoms.
Sources: NHS GMS, Literature
Mitochondrial disease v0.257 ACADS Bryony Thompson Marked gene: ACADS as ready
Mitochondrial disease v0.257 ACADS Bryony Thompson Gene: acads has been classified as Green List (High Evidence).
Mitochondrial disease v0.257 ACADS Bryony Thompson Classified gene: ACADS as Green List (high evidence)
Mitochondrial disease v0.257 ACADS Bryony Thompson Gene: acads has been classified as Green List (High Evidence).
Mitochondrial disease v0.256 ACADS Bryony Thompson gene: ACADS was added
gene: ACADS was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: ACADS was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ACADS were set to 25778941; 2808706; 29678161
Phenotypes for gene: ACADS were set to Acyl-CoA dehydrogenase, short-chain, deficiency of MIM#201470
Review for gene: ACADS was set to GREEN
Added comment: Short-chain acyl-CoA dehydrogenase deficiency (SCADD) is a rare autosomal recessive mitochondrial disorder of fatty acid β-oxidation. A defect in the substrate-generating upstream reactions of OXPHOS. >10 cases reported.
Sources: NHS GMS, Literature
Mitochondrial disease v0.255 ACADM Bryony Thompson Marked gene: ACADM as ready
Mitochondrial disease v0.255 ACADM Bryony Thompson Gene: acadm has been classified as Green List (High Evidence).
Mitochondrial disease v0.255 ACADM Bryony Thompson Classified gene: ACADM as Green List (high evidence)
Mitochondrial disease v0.255 ACADM Bryony Thompson Gene: acadm has been classified as Green List (High Evidence).
Mitochondrial disease v0.254 ACADM Bryony Thompson gene: ACADM was added
gene: ACADM was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: ACADM was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ACADM were set to 25778941; 1972503; 26223887
Phenotypes for gene: ACADM were set to Acyl-CoA dehydrogenase, medium chain, deficiency of MIM#201450
Review for gene: ACADM was set to GREEN
Added comment: Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is a disorder of mitochondrial fatty acid β-oxidation. A defect in the substrate-generating upstream reactions of OXPHOS. >3 cases reported.
Sources: NHS GMS, Literature
Mitochondrial disease v0.253 OXCT1 Bryony Thompson Marked gene: OXCT1 as ready
Mitochondrial disease v0.253 OXCT1 Bryony Thompson Gene: oxct1 has been classified as Green List (High Evidence).
Mitochondrial disease v0.253 OXCT1 Bryony Thompson Classified gene: OXCT1 as Green List (high evidence)
Mitochondrial disease v0.253 OXCT1 Bryony Thompson Gene: oxct1 has been classified as Green List (High Evidence).
Mitochondrial disease v0.252 OXCT1 Bryony Thompson gene: OXCT1 was added
gene: OXCT1 was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: OXCT1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: OXCT1 were set to 25778941; 10964512; 8751852; 23420214
Phenotypes for gene: OXCT1 were set to Succinyl CoA:3-oxoacid CoA transferase deficiency MIM#245050
Review for gene: OXCT1 was set to GREEN
Added comment: A mitochondrial matrix enzyme. Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency is a rare inherited metabolic disorder of ketone metabolism. A defect in the substrate-generating upstream reactions of OXPHOS. >3 cases reported.
Sources: NHS GMS, Literature
Mitochondrial disease v0.251 HMGCS2 Bryony Thompson Marked gene: HMGCS2 as ready
Mitochondrial disease v0.251 HMGCS2 Bryony Thompson Gene: hmgcs2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.251 HMGCS2 Bryony Thompson Classified gene: HMGCS2 as Green List (high evidence)
Mitochondrial disease v0.251 HMGCS2 Bryony Thompson Gene: hmgcs2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.250 HMGCS2 Bryony Thompson gene: HMGCS2 was added
gene: HMGCS2 was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: HMGCS2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: HMGCS2 were set to 25778941; 9337379; 23751782
Phenotypes for gene: HMGCS2 were set to HMG-CoA synthase-2 deficiency MIM#605911
Review for gene: HMGCS2 was set to GREEN
Added comment: Mitochondrial HMG-CoA synthase deficiency is a rare inherited metabolic disorder that affects ketone-body synthesis. A defect in the substrate-generating upstream reactions of OXPHOS. >3 cases reported.
Sources: NHS GMS, Literature
Mitochondrial disease v0.249 HMGCL Bryony Thompson Marked gene: HMGCL as ready
Mitochondrial disease v0.249 HMGCL Bryony Thompson Gene: hmgcl has been classified as Green List (High Evidence).
Mitochondrial disease v0.249 HMGCL Bryony Thompson Classified gene: HMGCL as Green List (high evidence)
Mitochondrial disease v0.249 HMGCL Bryony Thompson Gene: hmgcl has been classified as Green List (High Evidence).
Mitochondrial disease v0.248 HMGCL Bryony Thompson gene: HMGCL was added
gene: HMGCL was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: HMGCL was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: HMGCL were set to 25778941; 11129331; 19036343
Phenotypes for gene: HMGCL were set to HMG-CoA lyase deficiency MIM#246450
Review for gene: HMGCL was set to GREEN
Added comment: 3-Hydroxy-3-methylglutaric aciduria is a rare autosomal recessive genetic disorder due to a deficiency of the 3-hydroxy-3-methylglutarylCoA lyase (HMG-CoA lyase), a mitochondrial enzyme involved in ketogenesis and in the final step of l-leucine catabolism. A defect in the substrate-generating upstream reactions of OXPHOS. >3 cases reported.
Sources: NHS GMS, Literature
Mitochondrial disease v0.247 ACAT1 Bryony Thompson Classified gene: ACAT1 as Green List (high evidence)
Mitochondrial disease v0.247 ACAT1 Bryony Thompson Gene: acat1 has been classified as Green List (High Evidence).
Mitochondrial disease v0.246 ACAT1 Bryony Thompson gene: ACAT1 was added
gene: ACAT1 was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: ACAT1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ACAT1 were set to 31268215; 25778941; 1715688
Phenotypes for gene: ACAT1 were set to Alpha-methylacetoacetic aciduria MIM#203750
Review for gene: ACAT1 was set to GREEN
Added comment: Mitochondrial acetoacetyl-CoA thiolase deficiency is an inherited disorder of ketone body and isoleucine metabolism. A defect in the substrate-generating upstream reactions of OXPHOS. Over 100 cases reported.
Sources: NHS GMS, Literature
Mitochondrial disease v0.245 XPNPEP3 Bryony Thompson Marked gene: XPNPEP3 as ready
Mitochondrial disease v0.245 XPNPEP3 Bryony Thompson Gene: xpnpep3 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.245 XPNPEP3 Bryony Thompson Classified gene: XPNPEP3 as Amber List (moderate evidence)
Mitochondrial disease v0.245 XPNPEP3 Bryony Thompson Added comment: Comment on list classification: No other families reported since the two reported in 2010, and the animal model is a zebrafish rather than mouse, thus set to amber.
Mitochondrial disease v0.245 XPNPEP3 Bryony Thompson Gene: xpnpep3 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.244 XPNPEP3 Bryony Thompson gene: XPNPEP3 was added
gene: XPNPEP3 was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: XPNPEP3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: XPNPEP3 were set to 20179356; 25778941
Phenotypes for gene: XPNPEP3 were set to Nephronophthisis-like nephropathy 1 MIM#613159
Review for gene: XPNPEP3 was set to AMBER
Added comment: Two families with two different homozygous variants, and a zebrafish model. The protein localises to the mitochondria of renal cells and is involved in mitochondrial homeostasis. It belongs to a family of X-pro-aminopeptidases, and has a role in ciliary function.
Sources: NHS GMS, Literature
Mitochondrial disease v0.243 SLC25A20 Bryony Thompson Marked gene: SLC25A20 as ready
Mitochondrial disease v0.243 SLC25A20 Bryony Thompson Gene: slc25a20 has been classified as Green List (High Evidence).
Mitochondrial disease v0.243 SLC25A20 Bryony Thompson Classified gene: SLC25A20 as Green List (high evidence)
Mitochondrial disease v0.243 SLC25A20 Bryony Thompson Gene: slc25a20 has been classified as Green List (High Evidence).
Mitochondrial disease v0.242 SLC25A20 Bryony Thompson gene: SLC25A20 was added
gene: SLC25A20 was added to Mitochondrial disease. Sources: Literature,NHS GMS
Mode of inheritance for gene: SLC25A20 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC25A20 were set to 9399886; 31108048; 25778941
Phenotypes for gene: SLC25A20 were set to Carnitine-acylcarnitine translocase deficiency MIM#212138
Review for gene: SLC25A20 was set to GREEN
Added comment: >3 cases. Condition is a recessive disorder of mitochondrial fatty acid oxidation.
Sources: Literature, NHS GMS
Mitochondrial disease v0.241 SLC22A5 Bryony Thompson Classified gene: SLC22A5 as Green List (high evidence)
Mitochondrial disease v0.241 SLC22A5 Bryony Thompson Gene: slc22a5 has been classified as Green List (High Evidence).
Mitochondrial disease v0.240 SLC22A5 Bryony Thompson gene: SLC22A5 was added
gene: SLC22A5 was added to Mitochondrial disease. Sources: NHS GMS,Literature
Mode of inheritance for gene: SLC22A5 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC22A5 were set to 9916797; 25778941; 17884651
Phenotypes for gene: SLC22A5 were set to Carnitine deficiency, systemic primary MIM#212140
Review for gene: SLC22A5 was set to GREEN
Added comment: >3 cases and a mouse model. Protein has a function in carnitine-dependent oxidation of long-chain fatty acids in mitochondria and is essential for normal gut function.
Sources: NHS GMS, Literature
Mendeliome v0.1799 IDH3A Zornitza Stark Marked gene: IDH3A as ready
Mendeliome v0.1799 IDH3A Zornitza Stark Gene: idh3a has been classified as Green List (High Evidence).
Mendeliome v0.1799 IDH3A Zornitza Stark Classified gene: IDH3A as Green List (high evidence)
Mendeliome v0.1799 IDH3A Zornitza Stark Gene: idh3a has been classified as Green List (High Evidence).
Mendeliome v0.1798 IDH3A Zornitza Stark gene: IDH3A was added
gene: IDH3A was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: IDH3A was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: IDH3A were set to 31012789; 30478029; 30058936; 28412069
Phenotypes for gene: IDH3A were set to Retinitis pigmentosa
Review for gene: IDH3A was set to GREEN
Added comment: Six unrelated families reported with retinitis pigmentosa. Mouse model.
Sources: NHS GMS
Mitochondrial disease v0.239 IDH3A Zornitza Stark Classified gene: IDH3A as Green List (high evidence)
Mitochondrial disease v0.239 IDH3A Zornitza Stark Gene: idh3a has been classified as Green List (High Evidence).
Mitochondrial disease v0.238 IDH3A Zornitza Stark gene: IDH3A was added
gene: IDH3A was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: IDH3A was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: IDH3A were set to 31012789; 30478029; 30058936; 28412069
Phenotypes for gene: IDH3A were set to Retinitis pigmentosa
Review for gene: IDH3A was set to GREEN
Added comment: Six unrelated families reported with retinitis pigmentosa. Mouse model.
Sources: NHS GMS
Mitochondrial disease v0.237 HLCS Zornitza Stark Classified gene: HLCS as Green List (high evidence)
Mitochondrial disease v0.237 HLCS Zornitza Stark Gene: hlcs has been classified as Green List (High Evidence).
Mitochondrial disease v0.236 HLCS Zornitza Stark edited their review of gene: HLCS: Changed rating: GREEN
Mendeliome v0.1797 GATC Zornitza Stark Marked gene: GATC as ready
Mendeliome v0.1797 GATC Zornitza Stark Gene: gatc has been classified as Red List (Low Evidence).
Mendeliome v0.1797 GATC Zornitza Stark gene: GATC was added
gene: GATC was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: GATC was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GATC were set to 30283131
Phenotypes for gene: GATC were set to Mitochondrial cardiomyopathy
Review for gene: GATC was set to RED
Added comment: Two families with 6 affected individuals reported; same homozygous variant.
Sources: NHS GMS
Mitochondrial disease v0.236 GATC Zornitza Stark Marked gene: GATC as ready
Mitochondrial disease v0.236 GATC Zornitza Stark Gene: gatc has been classified as Red List (Low Evidence).
Mitochondrial disease v0.236 GATC Zornitza Stark gene: GATC was added
gene: GATC was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: GATC was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GATC were set to 30283131
Phenotypes for gene: GATC were set to Mitochondrial cardiomyopathy
Review for gene: GATC was set to RED
Added comment: Two families with 6 affected individuals reported; same homozygous variant.
Sources: NHS GMS
Mendeliome v0.1796 GATB Zornitza Stark Marked gene: GATB as ready
Mendeliome v0.1796 GATB Zornitza Stark Gene: gatb has been classified as Red List (Low Evidence).
Mendeliome v0.1796 GATB Zornitza Stark gene: GATB was added
gene: GATB was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: GATB was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GATB were set to 30283131
Phenotypes for gene: GATB were set to Mitochondrial cardiomyopathy
Review for gene: GATB was set to RED
Added comment: Single family reported with two affected siblings
Sources: NHS GMS
Mitochondrial disease v0.235 GATB Zornitza Stark Marked gene: GATB as ready
Mitochondrial disease v0.235 GATB Zornitza Stark Gene: gatb has been classified as Red List (Low Evidence).
Mitochondrial disease v0.235 GATB Zornitza Stark gene: GATB was added
gene: GATB was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: GATB was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GATB were set to 30283131
Phenotypes for gene: GATB were set to Mitochondrial cardiomyopathy
Review for gene: GATB was set to RED
Added comment: Single family reported with two affected siblings.
Sources: NHS GMS
Mitochondrial disease v0.234 SLC25A10 Bryony Thompson Classified gene: SLC25A10 as Amber List (moderate evidence)
Mitochondrial disease v0.234 SLC25A10 Bryony Thompson Gene: slc25a10 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.233 SLC25A10 Bryony Thompson gene: SLC25A10 was added
gene: SLC25A10 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: SLC25A10 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC25A10 were set to 29211846
Phenotypes for gene: SLC25A10 were set to Intractable epileptic encephalopathy
Review for gene: SLC25A10 was set to AMBER
Added comment: One case with intractable epileptic encephalopathy with complex I deficiency, with biallelic variants. Yeast SLC25A10 ortholog lack-of-function causes impairment in mitochondrial respiration, reduced mtDNA copy number and oxidative stress vulnerability
Sources: NHS GMS
Mendeliome v0.1795 EFTUD2 Elena Savva reviewed gene: EFTUD2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Mandibulofacial dysostosis, Guion-Almeida type 610536; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Mendeliome v0.1795 PAX1 Elena Savva reviewed gene: PAX1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 29681087, 28657137, 23851939; Phenotypes: ?Otofaciocervical syndrome 2; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1795 SHANK2 Elena Savva reviewed gene: SHANK2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 30072871, 30911184; Phenotypes: {Autism susceptibility 17}, Autism spectrum disorder with or without intellectual disability; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Mitochondrial disease v0.232 SLC25A21 Bryony Thompson Marked gene: SLC25A21 as ready
Mitochondrial disease v0.232 SLC25A21 Bryony Thompson Gene: slc25a21 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.232 SLC25A21 Bryony Thompson Classified gene: SLC25A21 as Amber List (moderate evidence)
Mitochondrial disease v0.232 SLC25A21 Bryony Thompson Gene: slc25a21 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.231 SLC25A21 Bryony Thompson gene: SLC25A21 was added
gene: SLC25A21 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: SLC25A21 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC25A21 were set to 29517768
Phenotypes for gene: SLC25A21 were set to Mitochondrial DNA depletion syndrome-18 MIM#618811
Review for gene: SLC25A21 was set to AMBER
Added comment: One case with a homozygous variant and functional assays showing mitochondrial dysfunction.
Sources: NHS GMS
Mitochondrial disease v0.230 SLC25A24 Bryony Thompson Marked gene: SLC25A24 as ready
Mitochondrial disease v0.230 SLC25A24 Bryony Thompson Gene: slc25a24 has been classified as Green List (High Evidence).
Mitochondrial disease v0.230 SLC25A24 Bryony Thompson Classified gene: SLC25A24 as Green List (high evidence)
Mitochondrial disease v0.230 SLC25A24 Bryony Thompson Gene: slc25a24 has been classified as Green List (High Evidence).
Mitochondrial disease v0.229 SLC25A24 Bryony Thompson gene: SLC25A24 was added
gene: SLC25A24 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: SLC25A24 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: SLC25A24 were set to 29100094; 29100093
Phenotypes for gene: SLC25A24 were set to Fontaine progeroid syndrome MIM#612289
Review for gene: SLC25A24 was set to GREEN
Added comment: De novo heterozygous variants (R217H, R217C) were identified in 9 unrelated cases. Functional analysis demonstrated that the variants affect mitochondrial morphology, and also suggested an impact on oxidative phosphorylation via decreased ATP synthesis and an increase in the mitochondrial membrane potential, thus creating conditions that are inhospitable to cell proliferation.
Sources: NHS GMS
Mendeliome v0.1795 IFT172 Elena Savva reviewed gene: IFT172: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 26763875; Phenotypes: Retinitis pigmentosa 71 616394, Short-rib thoracic dysplasia 10 with or without polydactyly - 615630, Bardet-Biedl syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.228 SLC39A8 Bryony Thompson Classified gene: SLC39A8 as Amber List (moderate evidence)
Mitochondrial disease v0.228 SLC39A8 Bryony Thompson Added comment: Comment on list classification: There's currently one family with a Leigh-like mitochondrial phenotype and in vitro functional assay data.
Mitochondrial disease v0.228 SLC39A8 Bryony Thompson Gene: slc39a8 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.227 SLC39A8 Zornitza Stark Marked gene: SLC39A8 as ready
Mitochondrial disease v0.227 SLC39A8 Zornitza Stark Gene: slc39a8 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.227 SLC39A8 Zornitza Stark Classified gene: SLC39A8 as Amber List (moderate evidence)
Mitochondrial disease v0.227 SLC39A8 Zornitza Stark Gene: slc39a8 has been classified as Amber List (Moderate Evidence).
Cataract v0.33 CD40LG Zornitza Stark Marked gene: CD40LG as ready
Cataract v0.33 CD40LG Zornitza Stark Gene: cd40lg has been classified as Red List (Low Evidence).
Cataract v0.33 CD40LG Zornitza Stark Phenotypes for gene: CD40LG were changed from to Immunodeficiency with Hyper-IgM type 1
Cataract v0.32 CD40LG Zornitza Stark Mode of inheritance for gene: CD40LG was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Cataract v0.32 CD40LG Zornitza Stark Classified gene: CD40LG as Red List (low evidence)
Cataract v0.32 CD40LG Zornitza Stark Gene: cd40lg has been classified as Red List (Low Evidence).
Cataract v0.31 CD3G Zornitza Stark Marked gene: CD3G as ready
Cataract v0.31 CD3G Zornitza Stark Gene: cd3g has been classified as Red List (Low Evidence).
Cataract v0.31 CD3G Zornitza Stark Phenotypes for gene: CD3G were changed from to Immunodeficiency 17, CD3 gamma deficient
Cataract v0.30 CD3G Zornitza Stark Publications for gene: CD3G were set to
Cataract v0.30 CD3G Zornitza Stark Classified gene: CD3G as Red List (low evidence)
Cataract v0.30 CD3G Zornitza Stark Gene: cd3g has been classified as Red List (Low Evidence).
Haem degradation and bilirubin metabolism defects v0.0 FECH Zornitza Stark Tag SV/CNV tag was added to gene: FECH.
Tag deep intronic tag was added to gene: FECH.
Haem degradation and bilirubin metabolism defects v0.0 FECH Zornitza Stark reviewed gene: FECH: Rating: GREEN; Mode of pathogenicity: None; Publications: 20105171, 23016163; Phenotypes: Protoporphyria, erythropoietic, 1, MIM# 177000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1795 FECH Zornitza Stark Marked gene: FECH as ready
Mendeliome v0.1795 FECH Zornitza Stark Added comment: Comment when marking as ready: Evidence for dominant disease is limited. Please note there is a common, hypomorphic deep intronic variant, IVS3-48T-C, as well as an exon 10 deletion reported.
Mendeliome v0.1795 FECH Zornitza Stark Gene: fech has been classified as Green List (High Evidence).
Mendeliome v0.1795 FECH Zornitza Stark Tag SV/CNV tag was added to gene: FECH.
Mitochondrial disease v0.226 SLC39A8 Bryony Thompson gene: SLC39A8 was added
gene: SLC39A8 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: SLC39A8 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC39A8 were set to 29453449; 27995398
Phenotypes for gene: SLC39A8 were set to Congenital disorder of glycosylation, type IIn MIM#616721
Review for gene: SLC39A8 was set to AMBER
Added comment: Functional analyses of loss of function variants that have been identified in 3 CDG type II-associated cases and a Leigh-like syndrome mitochondrial disorder case resulted in mitochondrial dysfunction and oxidative stress.
Sources: NHS GMS
Mendeliome v0.1795 FECH Zornitza Stark Phenotypes for gene: FECH were changed from to Protoporphyria, erythropoietic, 1 177000 AR
Mendeliome v0.1794 FECH Zornitza Stark Publications for gene: FECH were set to
Mendeliome v0.1793 FECH Zornitza Stark Mode of inheritance for gene: FECH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1792 FECH Zornitza Stark Tag deep intronic tag was added to gene: FECH.
Cataract v0.29 AICDA Zornitza Stark Marked gene: AICDA as ready
Cataract v0.29 AICDA Zornitza Stark Gene: aicda has been classified as Red List (Low Evidence).
Cataract v0.29 AICDA Zornitza Stark Phenotypes for gene: AICDA were changed from to Immunodeficiency with hyper-IgM, type 2 605258
Cataract v0.28 AICDA Zornitza Stark Publications for gene: AICDA were set to
Cataract v0.27 AICDA Zornitza Stark Classified gene: AICDA as Red List (low evidence)
Cataract v0.27 AICDA Zornitza Stark Gene: aicda has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2473 SPATA5 Zornitza Stark Phenotypes for gene: SPATA5 were changed from Epilepsy, hearing loss, and mental retardation syndrome MIM#616577 to Epilepsy, hearing loss, and mental retardation syndrome MIM#616577
Intellectual disability syndromic and non-syndromic v0.2473 SPATA5 Zornitza Stark Marked gene: SPATA5 as ready
Intellectual disability syndromic and non-syndromic v0.2473 SPATA5 Zornitza Stark Gene: spata5 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2473 SPATA5 Zornitza Stark Marked gene: SPATA5 as ready
Intellectual disability syndromic and non-syndromic v0.2473 SPATA5 Zornitza Stark Gene: spata5 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2473 SPATA5 Zornitza Stark Phenotypes for gene: SPATA5 were changed from to Epilepsy, hearing loss, and mental retardation syndrome MIM#616577
Intellectual disability syndromic and non-syndromic v0.2472 SPATA5 Zornitza Stark Publications for gene: SPATA5 were set to
Intellectual disability syndromic and non-syndromic v0.2471 SPATA5 Zornitza Stark Mode of inheritance for gene: SPATA5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2470 SPATA5 Zornitza Stark reviewed gene: SPATA5: Rating: GREEN; Mode of pathogenicity: None; Publications: 30009132, 29343804; Phenotypes: Epilepsy, hearing loss, and mental retardation syndrome MIM#616577; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1792 ADAM17 Zornitza Stark Marked gene: ADAM17 as ready
Mendeliome v0.1792 ADAM17 Zornitza Stark Added comment: Comment when marking as ready: Two families and a mouse model.
Mendeliome v0.1792 ADAM17 Zornitza Stark Gene: adam17 has been classified as Green List (High Evidence).
Mendeliome v0.1792 ADAM17 Zornitza Stark Phenotypes for gene: ADAM17 were changed from to Inflammatory neonatal-onset skin and bowel disease, MIM#614328
Mendeliome v0.1791 ADAM17 Zornitza Stark Publications for gene: ADAM17 were set to
Mendeliome v0.1790 ADAM17 Zornitza Stark Mode of inheritance for gene: ADAM17 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1789 ADAM17 Zornitza Stark Classified gene: ADAM17 as Green List (high evidence)
Mendeliome v0.1789 ADAM17 Zornitza Stark Gene: adam17 has been classified as Green List (High Evidence).
Cataract v0.26 ADAM17 Zornitza Stark Marked gene: ADAM17 as ready
Cataract v0.26 ADAM17 Zornitza Stark Gene: adam17 has been classified as Red List (Low Evidence).
Cataract v0.26 ADAM17 Zornitza Stark Phenotypes for gene: ADAM17 were changed from to Inflammatory skin and bowel disease
Cataract v0.25 ADAM17 Zornitza Stark Publications for gene: ADAM17 were set to
Cataract v0.24 ADAM17 Zornitza Stark Mode of inheritance for gene: ADAM17 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Cataract v0.23 ADAM17 Zornitza Stark Classified gene: ADAM17 as Red List (low evidence)
Cataract v0.23 ADAM17 Zornitza Stark Gene: adam17 has been classified as Red List (Low Evidence).
Rasopathy v0.15 PTPN11 Zornitza Stark Marked gene: PTPN11 as ready
Rasopathy v0.15 PTPN11 Zornitza Stark Gene: ptpn11 has been classified as Green List (High Evidence).
Rasopathy v0.15 PTPN11 Zornitza Stark Phenotypes for gene: PTPN11 were changed from to LEOPARD syndrome 1, 151100 AD (for reporting use Noonan syndrome with multiple lentigines); Metachondromatosis, 156250 AD; Noonan syndrome 1, 163950 AD; Leukemia, juvenile myelomonocytic, somatic, 607785
Rasopathy v0.14 PTPN11 Zornitza Stark Mode of pathogenicity for gene: PTPN11 was changed from to Other
Rasopathy v0.13 PTPN11 Zornitza Stark Publications for gene: PTPN11 were set to
Rasopathy v0.12 PTPN11 Zornitza Stark Mode of inheritance for gene: PTPN11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cataract v0.22 CD40LG Lauren Akesson reviewed gene: CD40LG: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Immunodeficiency with Hyper-IgM type 1; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Cataract v0.22 CD3G Lauren Akesson reviewed gene: CD3G: Rating: RED; Mode of pathogenicity: None; Publications: 31921117; Phenotypes: Immunodeficiency 17, CD3 gamma deficient; Mode of inheritance: None
Callosome v0.116 ZNF462 Zornitza Stark Marked gene: ZNF462 as ready
Callosome v0.116 ZNF462 Zornitza Stark Gene: znf462 has been classified as Green List (High Evidence).
Callosome v0.116 ZNF462 Zornitza Stark Phenotypes for gene: ZNF462 were changed from to Weiss-Kruszka syndrome, MIM#618619
Callosome v0.115 ZNF462 Zornitza Stark Publications for gene: ZNF462 were set to
Callosome v0.114 ZNF462 Zornitza Stark Mode of inheritance for gene: ZNF462 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Callosome v0.113 ZNF462 Zornitza Stark reviewed gene: ZNF462: Rating: GREEN; Mode of pathogenicity: None; Publications: 28513610, 31361404; Phenotypes: Weiss-Kruszka syndrome, MIM#618619; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1788 ZNF462 Zornitza Stark Marked gene: ZNF462 as ready
Mendeliome v0.1788 ZNF462 Zornitza Stark Added comment: Comment when marking as ready: Multiple congenital anomaly syndrome characterised by variable but usually mild global developmental delay and common craniofacial abnormalities, including ptosis, abnormal head shape, downslanting palpebral fissures, epicanthal folds, arched eyebrows, and short upturned nose. Many patients have hypotonia and feeding difficulties. A few patients show agenesis of the corpus callosum on brain imaging. Most cases occur sporadically, but there are rare familial cases that show highly variable expressivity in the phenotypic manifestations.
Mendeliome v0.1788 ZNF462 Zornitza Stark Gene: znf462 has been classified as Green List (High Evidence).
Mendeliome v0.1788 ZNF462 Zornitza Stark Publications for gene: ZNF462 were set to 28513610
Mendeliome v0.1787 ZNF462 Zornitza Stark Phenotypes for gene: ZNF462 were changed from to Weiss-Kruszka syndrome, MIM#618619
Mendeliome v0.1786 ZNF462 Zornitza Stark Publications for gene: ZNF462 were set to
Mendeliome v0.1785 ZNF462 Zornitza Stark Mode of inheritance for gene: ZNF462 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1784 HCFC1 Zornitza Stark Marked gene: HCFC1 as ready
Mendeliome v0.1784 HCFC1 Zornitza Stark Gene: hcfc1 has been classified as Green List (High Evidence).
Mendeliome v0.1784 HCFC1 Zornitza Stark Phenotypes for gene: HCFC1 were changed from to Mental retardation, X-linked 3 (methylmalonic acidemia and homocysteinemia, cblX type ) 309541
Mendeliome v0.1783 HCFC1 Zornitza Stark Publications for gene: HCFC1 were set to
Mendeliome v0.1782 HCFC1 Zornitza Stark Mode of inheritance for gene: HCFC1 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Ichthyosis v0.73 NIPAL4 Zornitza Stark Marked gene: NIPAL4 as ready
Ichthyosis v0.73 NIPAL4 Zornitza Stark Gene: nipal4 has been classified as Green List (High Evidence).
Ichthyosis v0.73 NIPAL4 Zornitza Stark Phenotypes for gene: NIPAL4 were changed from to Ichthyosis, congenital, autosomal recessive 6, MIM# 612281
Ichthyosis v0.72 NIPAL4 Zornitza Stark Publications for gene: NIPAL4 were set to
Ichthyosis v0.71 NIPAL4 Zornitza Stark Mode of inheritance for gene: NIPAL4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Cataract v0.22 ADA Zornitza Stark Marked gene: ADA as ready
Cataract v0.22 ADA Zornitza Stark Gene: ada has been classified as Red List (Low Evidence).
Cataract v0.22 ADA Zornitza Stark Phenotypes for gene: ADA were changed from to Severe combined immunodeficiency due to ADA deficiency 102700
Cataract v0.21 ADA Zornitza Stark Mode of inheritance for gene: ADA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Cataract v0.20 ADA Zornitza Stark Classified gene: ADA as Red List (low evidence)
Cataract v0.20 ADA Zornitza Stark Gene: ada has been classified as Red List (Low Evidence).
Mendeliome v0.1781 TFAM Zornitza Stark gene: TFAM was added
gene: TFAM was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: TFAM was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TFAM were set to 27448789; 29021295; 9500544
Phenotypes for gene: TFAM were set to Mitochondrial DNA depletion syndrome 15 (hepatocerebral type) MIM#617156
Review for gene: TFAM was set to AMBER
Added comment: One consanguineous family segregates a homozygous variant. Tfam knockout mouse has a mitochondrial cardiomyopathy phenotype and severe mtDNA depletion with abolished oxidative phosphorylation.
Sources: NHS GMS
Cataract v0.19 BTK Lauren Akesson reviewed gene: BTK: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: X-linked agammaglobulinemia, isolated growth hormone deficiency type III with agammaglobulinemia; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Mendeliome v0.1780 TIMM22 Zornitza Stark Marked gene: TIMM22 as ready
Mendeliome v0.1780 TIMM22 Zornitza Stark Gene: timm22 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1780 TIMM22 Zornitza Stark Classified gene: TIMM22 as Amber List (moderate evidence)
Mendeliome v0.1780 TIMM22 Zornitza Stark Gene: timm22 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1779 TIMM22 Zornitza Stark gene: TIMM22 was added
gene: TIMM22 was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: TIMM22 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TIMM22 were set to 30452684
Phenotypes for gene: TIMM22 were set to mitochondrial myopathy; hypotonia; gastroesophageal reflux disease
Review for gene: TIMM22 was set to AMBER
Added comment: One compound heterozygote case identified with supporting in vitro and patient cell functional assays.
Sources: NHS GMS
Mendeliome v0.1778 TIMMDC1 Zornitza Stark Marked gene: TIMMDC1 as ready
Mendeliome v0.1778 TIMMDC1 Zornitza Stark Gene: timmdc1 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1778 TIMMDC1 Zornitza Stark Tag deep intronic tag was added to gene: TIMMDC1.
Mendeliome v0.1778 TIMMDC1 Zornitza Stark Classified gene: TIMMDC1 as Amber List (moderate evidence)
Mendeliome v0.1778 TIMMDC1 Zornitza Stark Gene: timmdc1 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1777 TIMMDC1 Zornitza Stark gene: TIMMDC1 was added
gene: TIMMDC1 was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: TIMMDC1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TIMMDC1 were set to 28604674; 30981218
Phenotypes for gene: TIMMDC1 were set to Mitochondrial complex I deficiency, nuclear type 31 MIM#618251
Review for gene: TIMMDC1 was set to AMBER
Added comment: A deep intronic variant (c.597-1340A>G, only detectable by WGS) that causes a splicing aberration was identified in a homozygous state in 3 unrelated cases from different ethnic backgrounds. A patient with Leigh-like syndrome had a homozygous stopgain variant in PDHX and a homozygous stopgain variant in TIMMDC1 (p.Arg225*). The TIMMDC1 mutant protein could still rescue complex I assembly in TIMMDC1 knockout cells and the patient’s clinical phenotype was not clearly distinct from that of other patients with the same PDHX defect.
Sources: NHS GMS
Mitochondrial disease v0.225 TIMMDC1 Zornitza Stark Tag deep intronic tag was added to gene: TIMMDC1.
Mendeliome v0.1776 TMEM65 Zornitza Stark Marked gene: TMEM65 as ready
Mendeliome v0.1776 TMEM65 Zornitza Stark Gene: tmem65 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1776 TMEM65 Zornitza Stark Classified gene: TMEM65 as Amber List (moderate evidence)
Mendeliome v0.1776 TMEM65 Zornitza Stark Gene: tmem65 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1775 TMEM65 Zornitza Stark gene: TMEM65 was added
gene: TMEM65 was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: TMEM65 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TMEM65 were set to 28295037
Phenotypes for gene: TMEM65 were set to Mitochondrial encephalomyopathy
Review for gene: TMEM65 was set to AMBER
Added comment: One homozygous case with a mitochondrial encephalomyopathy and functional assays showing the protein is important for mitochondrial respiration and mtDNA copy number maintenance.
Sources: NHS GMS
Cataract v0.19 ANAPC1 Lauren Akesson reviewed gene: ANAPC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 31303264; Phenotypes: Rothmund-Thomson syndrome type 1; Mode of inheritance: None
Mitochondrial disease v0.225 SLC52A2 Bryony Thompson Marked gene: SLC52A2 as ready
Mitochondrial disease v0.225 SLC52A2 Bryony Thompson Gene: slc52a2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.225 SLC52A2 Bryony Thompson Classified gene: SLC52A2 as Green List (high evidence)
Mitochondrial disease v0.225 SLC52A2 Bryony Thompson Gene: slc52a2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.224 SLC52A2 Bryony Thompson gene: SLC52A2 was added
gene: SLC52A2 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: SLC52A2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC52A2 were set to 29053833; 29193829
Phenotypes for gene: SLC52A2 were set to Brown-Vialetto-Van Laere syndrome 2 MIM#614707
Review for gene: SLC52A2 was set to GREEN
Added comment: The phenotype of at least 7 cases resembles a phenotype similar to mitochondrial disorders, electron transport chain complex I and complex II activity were decreased in SLC52A2 patient fibroblasts, and Drosophila model implicates mitochondrial dysfunction as a downstream consequence of riboflavin transporter gene defects.
Sources: NHS GMS
Mitochondrial disease v0.223 SLC52A3 Bryony Thompson Marked gene: SLC52A3 as ready
Mitochondrial disease v0.223 SLC52A3 Bryony Thompson Gene: slc52a3 has been classified as Green List (High Evidence).
Mitochondrial disease v0.223 SLC52A3 Bryony Thompson Classified gene: SLC52A3 as Green List (high evidence)
Mitochondrial disease v0.223 SLC52A3 Bryony Thompson Gene: slc52a3 has been classified as Green List (High Evidence).
Mitochondrial disease v0.222 SLC52A3 Bryony Thompson gene: SLC52A3 was added
gene: SLC52A3 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: SLC52A3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC52A3 were set to 29053833; 29193829
Phenotypes for gene: SLC52A3 were set to Brown-Vialetto-Van Laere syndrome 1 MIM#211530
Review for gene: SLC52A3 was set to GREEN
Added comment: The phenotype of >10 cases resembles a phenotype similar to mitochondrial disorders and Drosophila model implicates mitochondrial dysfunction as a downstream consequence of riboflavin transporter gene defects.
Sources: NHS GMS
Mendeliome v0.1774 FECH Michelle Torres reviewed gene: FECH: Rating: GREEN; Mode of pathogenicity: None; Publications: 20105171, 23016163; Phenotypes: Protoporphyria, erythropoietic, 1 177000 AR; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes
Cataract v0.19 AICDA Lauren Akesson reviewed gene: AICDA: Rating: RED; Mode of pathogenicity: None; Publications: 11007475, 27789066, 27142677, 19575287; Phenotypes: ; Mode of inheritance: None
Mitochondrial disease v0.221 SPATA5 Bryony Thompson Marked gene: SPATA5 as ready
Mitochondrial disease v0.221 SPATA5 Bryony Thompson Gene: spata5 has been classified as Green List (High Evidence).
Mitochondrial disease v0.221 SPATA5 Bryony Thompson Classified gene: SPATA5 as Green List (high evidence)
Mitochondrial disease v0.221 SPATA5 Bryony Thompson Gene: spata5 has been classified as Green List (High Evidence).
Mitochondrial disease v0.220 SPATA5 Bryony Thompson gene: SPATA5 was added
gene: SPATA5 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: SPATA5 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SPATA5 were set to 30009132; 29343804
Phenotypes for gene: SPATA5 were set to Epilepsy, hearing loss, and mental retardation syndrome MIM#616577
Review for gene: SPATA5 was set to GREEN
Added comment: At least five cases with biallelic variants had a clinical presentation resembling a mitochondrial disorder. Functional assays showed SPATA5-deficient neurons had a significant imbalance in the mitochondrial fusion-fission rate, impaired energy production and short axons.
Sources: NHS GMS
Mendeliome v0.1774 ADAM17 Lauren Akesson reviewed gene: ADAM17: Rating: AMBER; Mode of pathogenicity: None; Publications: 22010916, 25804906, 21041656, 22236242; Phenotypes: Inflammatory neonatal-onset skin and bowel disease; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cataract v0.19 ADAM17 Lauren Akesson edited their review of gene: ADAM17: Changed publications: 22010916, 25804906, 21041656, 22236242
Cataract v0.19 ADAM17 Lauren Akesson reviewed gene: ADAM17: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Inflammatory skin and bowel disease; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.219 SSBP1 Bryony Thompson Marked gene: SSBP1 as ready
Mitochondrial disease v0.219 SSBP1 Bryony Thompson Gene: ssbp1 has been classified as Green List (High Evidence).
Mitochondrial disease v0.219 SSBP1 Bryony Thompson Classified gene: SSBP1 as Green List (high evidence)
Mitochondrial disease v0.219 SSBP1 Bryony Thompson Added comment: Comment on list classification: Cases associated with mtDNA depletion without accumulation of multiple deletions
Mitochondrial disease v0.219 SSBP1 Bryony Thompson Gene: ssbp1 has been classified as Green List (High Evidence).
Optic Atrophy v0.11 SSBP1 Bryony Thompson Classified gene: SSBP1 as Green List (high evidence)
Optic Atrophy v0.11 SSBP1 Bryony Thompson Gene: ssbp1 has been classified as Green List (High Evidence).
Optic Atrophy v0.10 SSBP1 Bryony Thompson gene: SSBP1 was added
gene: SSBP1 was added to Optic Atrophy. Sources: NHS GMS
Mode of inheritance for gene: SSBP1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: SSBP1 were set to 31298765; 31479473; 31550237; 31550240
Phenotypes for gene: SSBP1 were set to Optic atrophy with or without extraocular phenotypes
Review for gene: SSBP1 was set to GREEN
Added comment: At least 9 dominant families/cases and 1 recessive with optic atrophy with/without additional clinical features, including retinal macular dystrophy, sensorineural deafness, mitochondrial myopathy, and kidney failure. Supporting evidence in functional assays and zebrafish model.
Sources: NHS GMS
Rasopathy v0.11 PTPN11 Michelle Torres reviewed gene: PTPN11: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID: 11992261, PMID: 21533187, PMID: 24935154; Phenotypes: LEOPARD syndrome 1, 151100 AD (for reporting use Noonan syndrome with multiple lentigines), Metachondromatosis, 156250 AD, Noonan syndrome 1, 163950 AD, Leukemia, juvenile myelomonocytic, somatic, 607785; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Mendeliome v0.1774 SSBP1 Bryony Thompson Marked gene: SSBP1 as ready
Mendeliome v0.1774 SSBP1 Bryony Thompson Gene: ssbp1 has been classified as Green List (High Evidence).
Mendeliome v0.1774 SSBP1 Bryony Thompson Classified gene: SSBP1 as Green List (high evidence)
Mendeliome v0.1774 SSBP1 Bryony Thompson Gene: ssbp1 has been classified as Green List (High Evidence).
Mendeliome v0.1773 SSBP1 Bryony Thompson gene: SSBP1 was added
gene: SSBP1 was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: SSBP1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: SSBP1 were set to 31298765; 31479473; 31550237; 31550240
Phenotypes for gene: SSBP1 were set to Optic atrophy with or without extraocular phenotypes
Review for gene: SSBP1 was set to GREEN
Added comment: At least 9 dominant families/cases and 1 recessive with optic atrophy with/without additional clinical features, including retinal macular dystrophy, sensorineural deafness, mitochondrial myopathy, and kidney failure. Supporting evidence in functional assays and zebrafish model.
Sources: NHS GMS
Mitochondrial disease v0.218 SSBP1 Bryony Thompson gene: SSBP1 was added
gene: SSBP1 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: SSBP1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: SSBP1 were set to 31298765; 31479473; 31550237; 31550240
Phenotypes for gene: SSBP1 were set to Optic atrophy with or without extraocular phenotypes
Review for gene: SSBP1 was set to GREEN
Added comment: At least 9 dominant families/cases and 1 recessive with optic atrophy with/without additional clinical features, including retinal macular dystrophy, sensorineural deafness, mitochondrial myopathy, and kidney failure. Supporting evidence in functional assays and zebrafish model.
Sources: NHS GMS
Mendeliome v0.1772 ZNF462 Elena Savva reviewed gene: ZNF462: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 28513610; Phenotypes: Weiss-Kruszka syndrome, 618619; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Mendeliome v0.1772 HCFC1 Elena Savva reviewed gene: HCFC1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 23000143; Phenotypes: Mental retardation, X-linked 3 (methylmalonic acidemia and homocysteinemia, cblX type ) 309541; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Ichthyosis v0.70 NIPAL4 Michelle Torres reviewed gene: NIPAL4: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 17557927; Phenotypes: Ichthyosis, congenital, autosomal recessive 6 612281 AR; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cataract v0.19 ADA Lauren Akesson reviewed gene: ADA: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: SCID-ADA; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.217 TFAM Bryony Thompson Marked gene: TFAM as ready
Mitochondrial disease v0.217 TFAM Bryony Thompson Gene: tfam has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.217 TFAM Bryony Thompson Classified gene: TFAM as Amber List (moderate evidence)
Mitochondrial disease v0.217 TFAM Bryony Thompson Gene: tfam has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.216 TFAM Bryony Thompson gene: TFAM was added
gene: TFAM was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: TFAM was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TFAM were set to 27448789; 29021295; 9500544
Phenotypes for gene: TFAM were set to Mitochondrial DNA depletion syndrome 15 (hepatocerebral type) MIM#617156
Review for gene: TFAM was set to AMBER
Added comment: One consanguineous family segregates a homozygous variant. Tfam knockout mouse has a mitochondrial cardiomyopathy phenotype and severe mtDNA depletion with abolished oxidative phosphorylation.
Sources: NHS GMS
Mitochondrial disease v0.215 TIMM22 Bryony Thompson Classified gene: TIMM22 as Amber List (moderate evidence)
Mitochondrial disease v0.215 TIMM22 Bryony Thompson Gene: timm22 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.214 TIMM22 Bryony Thompson changed review comment from: One compound heterozygote case identified with supporting in vitro and patient cell functional assays.
Sources: NHS GMS; to: One compound heterozygote case identified with supporting in vitro and patient cell functional assays. No OMIM phenotype recorded.
Sources: NHS GMS
Mitochondrial disease v0.214 TIMM22 Bryony Thompson gene: TIMM22 was added
gene: TIMM22 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: TIMM22 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TIMM22 were set to 30452684
Phenotypes for gene: TIMM22 were set to hypotonia; gastroesophageal reflux disease
Review for gene: TIMM22 was set to AMBER
Added comment: One compound heterozygote case identified with supporting in vitro and patient cell functional assays.
Sources: NHS GMS
Mitochondrial disease v0.213 TIMMDC1 Bryony Thompson Classified gene: TIMMDC1 as Amber List (moderate evidence)
Mitochondrial disease v0.213 TIMMDC1 Bryony Thompson Gene: timmdc1 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.212 TIMMDC1 Bryony Thompson gene: TIMMDC1 was added
gene: TIMMDC1 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: TIMMDC1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TIMMDC1 were set to 28604674; 30981218
Phenotypes for gene: TIMMDC1 were set to Mitochondrial complex I deficiency, nuclear type 31 MIM#618251
Review for gene: TIMMDC1 was set to AMBER
Added comment: A deep intronic variant (c.597-1340A>G, only detectable by WGS) that causes a splicing aberration was identified in a homozygous state in 3 unrelated cases from different ethnic backgrounds. A patient with Leigh-like syndrome had a homozygous stopgain variant in PDHX and a homozygous stopgain variant in TIMMDC1 (p.Arg225*). The TIMMDC1 mutant protein could still rescue complex I assembly in TIMMDC1 knockout cells and the patient’s clinical phenotype was not clearly distinct from that of other patients with the same PDHX defect.
Sources: NHS GMS
Mitochondrial disease v0.211 TMEM65 Bryony Thompson Classified gene: TMEM65 as Amber List (moderate evidence)
Mitochondrial disease v0.211 TMEM65 Bryony Thompson Gene: tmem65 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.210 TMEM65 Bryony Thompson edited their review of gene: TMEM65: Changed rating: AMBER
Mitochondrial disease v0.210 TMEM65 Bryony Thompson changed review comment from: One homozygous case with a mitochondrial encephalomyopathy and functional assays showing the protein is important for mitochondrial respiration and mtDNA copy number maintenance. Currently no OMIM or Gene2Phenotype phenotype entries.
Sources: NHS GMS; to: One homozygous case with a mitochondrial encephalomyopathy and functional assays showing the protein is important for mitochondrial respiration and mtDNA copy number maintenance. Currently no OMIM or Gene2Phenotype phenotype entries.
Sources: NHS GMS
Mitochondrial disease v0.210 TMEM65 Bryony Thompson gene: TMEM65 was added
gene: TMEM65 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: TMEM65 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TMEM65 were set to 28295037
Phenotypes for gene: TMEM65 were set to Mitochondrial encephalomyopathy
Added comment: One homozygous case with a mitochondrial encephalomyopathy and functional assays showing the protein is important for mitochondrial respiration and mtDNA copy number maintenance. Currently no OMIM or Gene2Phenotype phenotype entries.
Sources: NHS GMS
Mendeliome v0.1772 COX6A2 Zornitza Stark Marked gene: COX6A2 as ready
Mendeliome v0.1772 COX6A2 Zornitza Stark Gene: cox6a2 has been classified as Green List (High Evidence).
Mendeliome v0.1772 COX6A2 Zornitza Stark Classified gene: COX6A2 as Green List (high evidence)
Mendeliome v0.1772 COX6A2 Zornitza Stark Gene: cox6a2 has been classified as Green List (High Evidence).
Mendeliome v0.1771 COX6A2 Zornitza Stark gene: COX6A2 was added
gene: COX6A2 was added to Mendeliome. Sources: Expert list
Mode of inheritance for gene: COX6A2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: COX6A2 were set to 31155743; 23460811
Phenotypes for gene: COX6A2 were set to Mitochondrial complex IV deficiency, MIM# 220110
Review for gene: COX6A2 was set to GREEN
Added comment: Two unrelated families and two mouse models.
Sources: Expert list
Mitochondrial disease v0.209 COX6A2 Zornitza Stark Classified gene: COX6A2 as Green List (high evidence)
Mitochondrial disease v0.209 COX6A2 Zornitza Stark Gene: cox6a2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.209 COX6A2 Zornitza Stark Marked gene: COX6A2 as ready
Mitochondrial disease v0.209 COX6A2 Zornitza Stark Gene: cox6a2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.209 COX6A2 Zornitza Stark Classified gene: COX6A2 as Green List (high evidence)
Mitochondrial disease v0.209 COX6A2 Zornitza Stark Gene: cox6a2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.208 COX6A2 Zornitza Stark gene: COX6A2 was added
gene: COX6A2 was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: COX6A2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: COX6A2 were set to 31155743; 23460811
Phenotypes for gene: COX6A2 were set to Mitochondrial complex IV deficiency, MIM# 220110
Review for gene: COX6A2 was set to GREEN
Added comment: Two unrelated families and two mouse models.
Sources: Expert list
Mitochondrial disease v0.207 USMG5 Bryony Thompson Classified gene: USMG5 as Amber List (moderate evidence)
Mitochondrial disease v0.207 USMG5 Bryony Thompson Added comment: Comment on list classification: Currently only one potential Ashkenazi Jewish founder reported so far.
Mitochondrial disease v0.207 USMG5 Bryony Thompson Gene: usmg5 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.207 USMG5 Bryony Thompson Classified gene: USMG5 as Amber List (moderate evidence)
Mitochondrial disease v0.207 USMG5 Bryony Thompson Added comment: Comment on list classification: Currently only one potential Ashkenazi Jewish founder reported so far.
Mitochondrial disease v0.207 USMG5 Bryony Thompson Gene: usmg5 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.206 USMG5 Bryony Thompson gene: USMG5 was added
gene: USMG5 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: USMG5 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: USMG5 were set to 29917077; 30240627
Phenotypes for gene: USMG5 were set to Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6 MIM#618683
Review for gene: USMG5 was set to AMBER
Added comment: A homozygous splice site mutation in 4 patients from 3 unrelated families of Ashkenazi Jewish descent. Experimental analyses demonstrated that the splice variant leads to loss of protein expression and haplotype analysis suggested a founder effect. In situ cryo-ET analysis of the mitochondria of a homozygous affected case showed profound disturbances of mitochondrial crista ultrastructure.
Sources: NHS GMS
Mitochondrial disease v0.205 APTX Zornitza Stark Marked gene: APTX as ready
Mitochondrial disease v0.205 APTX Zornitza Stark Gene: aptx has been classified as Green List (High Evidence).
Mitochondrial disease v0.205 COA7 Zornitza Stark Marked gene: COA7 as ready
Mitochondrial disease v0.205 COA7 Zornitza Stark Gene: coa7 has been classified as Green List (High Evidence).
Mitochondrial disease v0.205 COQ7 Zornitza Stark Marked gene: COQ7 as ready
Mitochondrial disease v0.205 COQ7 Zornitza Stark Gene: coq7 has been classified as Green List (High Evidence).
Mitochondrial disease v0.205 ETFDH Zornitza Stark Marked gene: ETFDH as ready
Mitochondrial disease v0.205 ETFDH Zornitza Stark Gene: etfdh has been classified as Green List (High Evidence).
Mitochondrial disease v0.205 MRPS34 Zornitza Stark Marked gene: MRPS34 as ready
Mitochondrial disease v0.205 MRPS34 Zornitza Stark Gene: mrps34 has been classified as Green List (High Evidence).
Mitochondrial disease v0.205 ATP5A1 Zornitza Stark Marked gene: ATP5A1 as ready
Mitochondrial disease v0.205 ATP5A1 Zornitza Stark Gene: atp5a1 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.205 ATP5A1 Zornitza Stark Phenotypes for gene: ATP5A1 were changed from to Combined oxidative phosphorylation deficiency 22 616045; Mitochondrial complex V (ATP synthase) deficiency nuclear type 4, 615228
Mitochondrial disease v0.204 ATP5A1 Zornitza Stark Publications for gene: ATP5A1 were set to
Mitochondrial disease v0.203 TARS2 Zornitza Stark Marked gene: TARS2 as ready
Mitochondrial disease v0.203 TARS2 Zornitza Stark Gene: tars2 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.203 ATP5E Zornitza Stark Marked gene: ATP5E as ready
Mitochondrial disease v0.203 ATP5E Zornitza Stark Gene: atp5e has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.203 ATP5E Zornitza Stark Phenotypes for gene: ATP5E were changed from to Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3 MIM#614053
Mitochondrial disease v0.202 ATP5E Zornitza Stark Publications for gene: ATP5E were set to
Mitochondrial disease v0.201 ATP5E Zornitza Stark Mode of inheritance for gene: ATP5E was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.200 Zornitza Stark Panel types changed to Australian Genomics; Victorian Clinical Genetics Services; Royal Melbourne Hospital
Mendeliome v0.1770 YME1L1 Zornitza Stark Marked gene: YME1L1 as ready
Mendeliome v0.1770 YME1L1 Zornitza Stark Gene: yme1l1 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1770 YME1L1 Zornitza Stark Classified gene: YME1L1 as Amber List (moderate evidence)
Mendeliome v0.1770 YME1L1 Zornitza Stark Gene: yme1l1 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1769 YME1L1 Zornitza Stark gene: YME1L1 was added
gene: YME1L1 was added to Mendeliome. Sources: NHS GMS
Mode of inheritance for gene: YME1L1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: YME1L1 were set to 30544562; 27495975
Phenotypes for gene: YME1L1 were set to Optic atrophy 11, MIM#617302
Review for gene: YME1L1 was set to AMBER
Added comment: One consanguineous family with a homozygous variant and functional assays. YME1L leads to mitochondrial fragmentation and severely disorganized and attenuated cristae architecture in in vitro functional assays.
Sources: NHS GMS
Mitochondrial disease v0.199 COQ5 Zornitza Stark Marked gene: COQ5 as ready
Mitochondrial disease v0.199 COQ5 Zornitza Stark Gene: coq5 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.199 COQ5 Zornitza Stark gene: COQ5 was added
gene: COQ5 was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: COQ5 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: COQ5 were set to 29044765
Phenotypes for gene: COQ5 were set to Cerebellar ataxia; encephalopathy; generalized tonic-clonic seizures; intellectual disability
Review for gene: COQ5 was set to RED
Added comment: Three siblings reported, bi-allelic duplications in gene, said to lead to reduced CoQ10.
Sources: Expert list
Mitochondrial disease v0.198 CEP89 Zornitza Stark edited their review of gene: CEP89: Changed rating: RED
Mitochondrial disease v0.198 YME1L1 Bryony Thompson Classified gene: YME1L1 as Amber List (moderate evidence)
Mitochondrial disease v0.198 YME1L1 Bryony Thompson Gene: yme1l1 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.198 YME1L1 Bryony Thompson Classified gene: YME1L1 as Amber List (moderate evidence)
Mitochondrial disease v0.198 YME1L1 Bryony Thompson Gene: yme1l1 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.197 YME1L1 Bryony Thompson Marked gene: YME1L1 as ready
Mitochondrial disease v0.197 YME1L1 Bryony Thompson Gene: yme1l1 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.197 YME1L1 Bryony Thompson gene: YME1L1 was added
gene: YME1L1 was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: YME1L1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: YME1L1 were set to 30544562; 27495975
Phenotypes for gene: YME1L1 were set to Optic atrophy 11 MIM#617302
Review for gene: YME1L1 was set to AMBER
Added comment: One consanguineous family with a homozygous variant and functional assays. YME1L leads to mitochondrial fragmentation and severely disorganized and attenuated cristae architecture in in vitro functional assays.
Sources: NHS GMS
Mendeliome v0.1767 Bryony Thompson removed gene:ANXA11 from the panel
Mendeliome v0.1766 ANXA11 Bryony Thompson gene: ANXA11 was added
gene: ANXA11 was added to Mendeliome. Sources: Expert list
Mode of inheritance for gene: ANXA11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: ANXA11 were set to 28469040; 29845112; 30109997
Phenotypes for gene: ANXA11 were set to Amytrophic lateral sclerosis 23 MIM#617839
Review for gene: ANXA11 was set to GREEN
Added comment: 4 different missense variants in 10 patients from 7 unrelated families with amyotrophic lateral sclerosis and functional assays supporting association.
Sources: Expert list
Motor Neurone Disease v0.12 ANXA11 Bryony Thompson gene: ANXA11 was added
gene: ANXA11 was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: ANXA11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: ANXA11 were set to 28469040; 29845112; 30109997
Phenotypes for gene: ANXA11 were set to Amytrophic lateral sclerosis 23 MIM#617839
Review for gene: ANXA11 was set to GREEN
Added comment: 4 different missense variants in 10 patients from 7 unrelated families with amyotrophic lateral sclerosis and functional assays supporting association.
Sources: Expert list
Motor Neurone Disease v0.11 AIFM1 Bryony Thompson Classified gene: AIFM1 as Red List (low evidence)
Motor Neurone Disease v0.11 AIFM1 Bryony Thompson Added comment: Comment on list classification: Motor neuron degeneration is not a prominent feature of the condition. Only one case reported.
Motor Neurone Disease v0.11 AIFM1 Bryony Thompson Gene: aifm1 has been classified as Red List (Low Evidence).
Deafness_IsolatedAndComplex v0.329 PLOD3 Zornitza Stark Marked gene: PLOD3 as ready
Deafness_IsolatedAndComplex v0.329 PLOD3 Zornitza Stark Gene: plod3 has been classified as Green List (High Evidence).
Deafness_IsolatedAndComplex v0.329 PLOD3 Zornitza Stark Classified gene: PLOD3 as Green List (high evidence)
Deafness_IsolatedAndComplex v0.329 PLOD3 Zornitza Stark Gene: plod3 has been classified as Green List (High Evidence).
Deafness_IsolatedAndComplex v0.328 PLOD3 Lauren Akesson gene: PLOD3 was added
gene: PLOD3 was added to Deafness. Sources: Literature
Mode of inheritance for gene: PLOD3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PLOD3 were set to 18834968; 31129566
Phenotypes for gene: PLOD3 were set to Sensorineural deafness
Penetrance for gene: PLOD3 were set to unknown
Review for gene: PLOD3 was set to GREEN
Added comment: This gene has a complex phenotype that includes features of a connective tissue disorder; 3/5 described unrelated families have sensorineural deafness as a feature (PMID as above plus an abstract from 2013 ESHG by Steichen-Gersdorf et al). At least one proband has required cochlear implantation.
Sources: Literature
Stickler Syndrome v0.3 PLOD3 Zornitza Stark Marked gene: PLOD3 as ready
Stickler Syndrome v0.3 PLOD3 Zornitza Stark Gene: plod3 has been classified as Green List (High Evidence).
Stickler Syndrome v0.3 PLOD3 Zornitza Stark Classified gene: PLOD3 as Green List (high evidence)
Stickler Syndrome v0.3 PLOD3 Zornitza Stark Gene: plod3 has been classified as Green List (High Evidence).
Cataract v0.19 PLOD3 Zornitza Stark Marked gene: PLOD3 as ready
Cataract v0.19 PLOD3 Zornitza Stark Added comment: Comment when marking as ready: Borderline Green, unclear at present what proportion of affected individuals will have cataract as part of the phenotype.
Cataract v0.19 PLOD3 Zornitza Stark Gene: plod3 has been classified as Green List (High Evidence).
Cataract v0.19 PLOD3 Zornitza Stark Classified gene: PLOD3 as Green List (high evidence)
Cataract v0.19 PLOD3 Zornitza Stark Gene: plod3 has been classified as Green List (High Evidence).
Epidermolysis bullosa v0.24 PLOD3 Zornitza Stark Marked gene: PLOD3 as ready
Epidermolysis bullosa v0.24 PLOD3 Zornitza Stark Added comment: Comment when marking as ready: Agree, at present unclear what proportion of affected individuals have EB phenotype.
Epidermolysis bullosa v0.24 PLOD3 Zornitza Stark Gene: plod3 has been classified as Amber List (Moderate Evidence).
Epidermolysis bullosa v0.24 PLOD3 Zornitza Stark Classified gene: PLOD3 as Amber List (moderate evidence)
Epidermolysis bullosa v0.24 PLOD3 Zornitza Stark Gene: plod3 has been classified as Amber List (Moderate Evidence).
Stickler Syndrome v0.2 PLOD3 Lauren Akesson gene: PLOD3 was added
gene: PLOD3 was added to Stickler Syndrome. Sources: Literature
Mode of inheritance for gene: PLOD3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PLOD3 were set to 18834968; 30237576; 30463024; 31129566
Phenotypes for gene: PLOD3 were set to Stickler-like phenotype with high myopia, midface hypoplasia, microretrognathia
Penetrance for gene: PLOD3 were set to unknown
Review for gene: PLOD3 was set to GREEN
Added comment: Complex phenotype that includes features of a Stickler-like syndrome.
High myopia described in 3/5 described unrelated families
One description of retinal detachment
Facial dysmorphism with midface hypoplasia, microretrognathia

Other features include developmental delay and sensorineural hearing loss
Sources: Literature
Cataract v0.18 PLOD3 Lauren Akesson gene: PLOD3 was added
gene: PLOD3 was added to Cataract. Sources: Literature
Mode of inheritance for gene: PLOD3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PLOD3 were set to 18834968; 30463024; 31129566
Phenotypes for gene: PLOD3 were set to cataract
Penetrance for gene: PLOD3 were set to unknown
Review for gene: PLOD3 was set to GREEN
Added comment: Complex phenotype that includes cataracts in 3/5 described unrelated families
Sources: Literature
Epidermolysis bullosa v0.23 PLOD3 Lauren Akesson gene: PLOD3 was added
gene: PLOD3 was added to Epidermolysis bullosa. Sources: Literature
Mode of inheritance for gene: PLOD3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PLOD3 were set to 18834968; 30463024
Phenotypes for gene: PLOD3 were set to Blistering skin lesions
Penetrance for gene: PLOD3 were set to unknown
Review for gene: PLOD3 was set to AMBER
Added comment: Two unrelated families with complex phenotype
-18834968 with global developmental delay, facial dysmorphism, myopia, skeletal changes, blistering of toes, fingers and pinnae from infancy to age 5 years
- 30463024 with developmental delay, facial dysmorphism, myopia, diaphragmatic eventration, skeletal changes, haemorrhagic blisters and erosions

- A further 3 families with biallelic variants in this gene also had a complex phenotype that did not include blistering skin

As there are only two unrelated families with Epidermolysis Bullosa-like skin changes, this gene does not meet criteria for a gene-disease association.
Sources: Literature
Mendeliome v0.1765 UQCRQ Zornitza Stark Marked gene: UQCRQ as ready
Mendeliome v0.1765 UQCRQ Zornitza Stark Gene: uqcrq has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.196 VPS13C Zornitza Stark Marked gene: VPS13C as ready
Mitochondrial disease v0.196 VPS13C Zornitza Stark Gene: vps13c has been classified as Green List (High Evidence).
Mitochondrial disease v0.196 VPS13C Zornitza Stark Phenotypes for gene: VPS13C were changed from to Early-onset Parkinson disease-23, MIM# 616840
Mitochondrial disease v0.195 VPS13C Zornitza Stark Publications for gene: VPS13C were set to
Mitochondrial disease v0.194 VPS13C Zornitza Stark Mode of inheritance for gene: VPS13C was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.193 VPS13C Zornitza Stark reviewed gene: VPS13C: Rating: GREEN; Mode of pathogenicity: None; Publications: 26942284; Phenotypes: Early-onset Parkinson disease-23, MIM# 616840; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1765 UQCRQ Zornitza Stark Phenotypes for gene: UQCRQ were changed from to Mitochondrial complex III deficiency, nuclear type 4, MIM# 615159
Mendeliome v0.1764 UQCRQ Zornitza Stark Publications for gene: UQCRQ were set to
Mendeliome v0.1763 UQCRQ Zornitza Stark Mode of inheritance for gene: UQCRQ was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1762 UQCRQ Zornitza Stark Classified gene: UQCRQ as Amber List (moderate evidence)
Mendeliome v0.1762 UQCRQ Zornitza Stark Gene: uqcrq has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1761 UQCRQ Zornitza Stark reviewed gene: UQCRQ: Rating: AMBER; Mode of pathogenicity: None; Publications: 18439546; Phenotypes: Mitochondrial complex III deficiency, nuclear type 4, MIM# 615159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Callosome v0.113 UQCRQ Zornitza Stark Marked gene: UQCRQ as ready
Callosome v0.113 UQCRQ Zornitza Stark Gene: uqcrq has been classified as Red List (Low Evidence).
Callosome v0.113 UQCRQ Zornitza Stark Phenotypes for gene: UQCRQ were changed from to Mitochondrial complex III deficiency, nuclear type 4, MIM# 615159
Mitochondrial disease v0.193 UQCRQ Zornitza Stark Marked gene: UQCRQ as ready
Mitochondrial disease v0.193 UQCRQ Zornitza Stark Gene: uqcrq has been classified as Amber List (Moderate Evidence).
Callosome v0.112 UQCRQ Zornitza Stark Publications for gene: UQCRQ were set to
Mitochondrial disease v0.193 UQCRQ Zornitza Stark Phenotypes for gene: UQCRQ were changed from to Mitochondrial complex III deficiency, nuclear type 4, MIM# 615159
Callosome v0.111 UQCRQ Zornitza Stark Mode of inheritance for gene: UQCRQ was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Callosome v0.110 UQCRQ Zornitza Stark Classified gene: UQCRQ as Red List (low evidence)
Callosome v0.110 UQCRQ Zornitza Stark Gene: uqcrq has been classified as Red List (Low Evidence).
Callosome v0.109 UQCRQ Zornitza Stark reviewed gene: UQCRQ: Rating: RED; Mode of pathogenicity: None; Publications: 18439546; Phenotypes: Mitochondrial complex III deficiency, nuclear type 4, MIM# 615159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.192 UQCRQ Zornitza Stark Publications for gene: UQCRQ were set to
Mitochondrial disease v0.191 UQCRQ Zornitza Stark Mode of inheritance for gene: UQCRQ was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.190 UQCRQ Zornitza Stark Classified gene: UQCRQ as Amber List (moderate evidence)
Mitochondrial disease v0.190 UQCRQ Zornitza Stark Gene: uqcrq has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.189 UQCRQ Zornitza Stark reviewed gene: UQCRQ: Rating: AMBER; Mode of pathogenicity: None; Publications: 18439546; Phenotypes: Mitochondrial complex III deficiency, nuclear type 4, MIM# 615159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1761 UQCRC2 Zornitza Stark Marked gene: UQCRC2 as ready
Mendeliome v0.1761 UQCRC2 Zornitza Stark Gene: uqcrc2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1761 UQCRC2 Zornitza Stark Phenotypes for gene: UQCRC2 were changed from to Mitochondrial complex III deficiency, nuclear type 5, MIM# 615160
Mendeliome v0.1760 UQCRC2 Zornitza Stark Publications for gene: UQCRC2 were set to
Mendeliome v0.1759 UQCRC2 Zornitza Stark Mode of inheritance for gene: UQCRC2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1758 UQCRC2 Zornitza Stark Classified gene: UQCRC2 as Amber List (moderate evidence)
Mendeliome v0.1758 UQCRC2 Zornitza Stark Gene: uqcrc2 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.189 UQCRC2 Zornitza Stark Marked gene: UQCRC2 as ready
Mitochondrial disease v0.189 UQCRC2 Zornitza Stark Gene: uqcrc2 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.189 UQCRC2 Zornitza Stark Phenotypes for gene: UQCRC2 were changed from to Mitochondrial complex III deficiency, nuclear type 5, MIM# 615160
Mendeliome v0.1757 UQCRC2 Zornitza Stark reviewed gene: UQCRC2: Rating: AMBER; Mode of pathogenicity: None; Publications: 28275242, 23281071; Phenotypes: Mitochondrial complex III deficiency, nuclear type 5, MIM# 615160; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.188 UQCRC2 Zornitza Stark Publications for gene: UQCRC2 were set to
Mitochondrial disease v0.187 UQCRC2 Zornitza Stark Classified gene: UQCRC2 as Amber List (moderate evidence)
Mitochondrial disease v0.187 UQCRC2 Zornitza Stark Gene: uqcrc2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1757 UQCC3 Zornitza Stark Marked gene: UQCC3 as ready
Mendeliome v0.1757 UQCC3 Zornitza Stark Gene: uqcc3 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.186 UQCRC2 Zornitza Stark reviewed gene: UQCRC2: Rating: AMBER; Mode of pathogenicity: None; Publications: 28275242, 23281071; Phenotypes: Mitochondrial complex III deficiency, nuclear type 5, MIM# 615160; Mode of inheritance: None
Mendeliome v0.1757 UQCC3 Zornitza Stark Phenotypes for gene: UQCC3 were changed from to Mitochondrial complex III deficiency, nuclear type 9, MIM# 616111
Mitochondrial disease v0.186 UQCC3 Zornitza Stark Marked gene: UQCC3 as ready
Mitochondrial disease v0.186 UQCC3 Zornitza Stark Gene: uqcc3 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.186 UQCC3 Zornitza Stark Phenotypes for gene: UQCC3 were changed from to Mitochondrial complex III deficiency, nuclear type 9, MIM# 616111
Mendeliome v0.1756 UQCC3 Zornitza Stark Publications for gene: UQCC3 were set to
Mendeliome v0.1755 UQCC3 Zornitza Stark Mode of inheritance for gene: UQCC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1754 UQCC3 Zornitza Stark Classified gene: UQCC3 as Amber List (moderate evidence)
Mendeliome v0.1754 UQCC3 Zornitza Stark Gene: uqcc3 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.185 UQCC3 Zornitza Stark Publications for gene: UQCC3 were set to
Mendeliome v0.1753 UQCC3 Zornitza Stark reviewed gene: UQCC3: Rating: AMBER; Mode of pathogenicity: None; Publications: 25008109, 28804536; Phenotypes: Mitochondrial complex III deficiency, nuclear type 9, MIM# 616111; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.184 UQCC3 Zornitza Stark Mode of inheritance for gene: UQCC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.183 UQCC3 Zornitza Stark Classified gene: UQCC3 as Amber List (moderate evidence)
Mitochondrial disease v0.183 UQCC3 Zornitza Stark Gene: uqcc3 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.182 UQCC3 Zornitza Stark reviewed gene: UQCC3: Rating: AMBER; Mode of pathogenicity: None; Publications: 25008109, 28804536; Phenotypes: Mitochondrial complex III deficiency, nuclear type 9, MIM# 616111; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1753 TXN2 Zornitza Stark Marked gene: TXN2 as ready
Mendeliome v0.1753 TXN2 Zornitza Stark Gene: txn2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1753 TXN2 Zornitza Stark Phenotypes for gene: TXN2 were changed from to Combined oxidative phosphorylation deficiency 29, MIM# 616811
Mitochondrial disease v0.182 TXN2 Zornitza Stark Marked gene: TXN2 as ready
Mitochondrial disease v0.182 TXN2 Zornitza Stark Gene: txn2 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.182 TXN2 Zornitza Stark Phenotypes for gene: TXN2 were changed from to Combined oxidative phosphorylation deficiency 29, MIM# 616811
Mendeliome v0.1752 TXN2 Zornitza Stark Publications for gene: TXN2 were set to
Mitochondrial disease v0.181 TXN2 Zornitza Stark Publications for gene: TXN2 were set to
Mendeliome v0.1751 TXN2 Zornitza Stark Mode of inheritance for gene: TXN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1750 TXN2 Zornitza Stark Classified gene: TXN2 as Amber List (moderate evidence)
Mendeliome v0.1750 TXN2 Zornitza Stark Gene: txn2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1749 TXN2 Zornitza Stark reviewed gene: TXN2: Rating: AMBER; Mode of pathogenicity: None; Publications: 26626369, 12529397; Phenotypes: Combined oxidative phosphorylation deficiency 29, MIM# 616811; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.180 TXN2 Zornitza Stark Mode of inheritance for gene: TXN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.179 TXN2 Zornitza Stark Classified gene: TXN2 as Amber List (moderate evidence)
Mitochondrial disease v0.179 TXN2 Zornitza Stark Gene: txn2 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.178 TXN2 Zornitza Stark reviewed gene: TXN2: Rating: AMBER; Mode of pathogenicity: None; Publications: 26626369, 12529397; Phenotypes: Combined oxidative phosphorylation deficiency 29, MIM# 616811; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1749 TARS2 Zornitza Stark Marked gene: TARS2 as ready
Mendeliome v0.1749 TARS2 Zornitza Stark Gene: tars2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1749 TARS2 Zornitza Stark Phenotypes for gene: TARS2 were changed from to Combined oxidative phosphorylation deficiency 21, MIM# 615918
Mendeliome v0.1748 TARS2 Zornitza Stark Publications for gene: TARS2 were set to
Mendeliome v0.1747 TARS2 Zornitza Stark Mode of inheritance for gene: TARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1746 TARS2 Zornitza Stark Classified gene: TARS2 as Amber List (moderate evidence)
Mendeliome v0.1746 TARS2 Zornitza Stark Gene: tars2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1745 TARS2 Zornitza Stark reviewed gene: TARS2: Rating: AMBER; Mode of pathogenicity: None; Publications: 24827421, 26811336; Phenotypes: Combined oxidative phosphorylation deficiency 21, MIM# 615918; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.178 TARS2 Zornitza Stark Phenotypes for gene: TARS2 were changed from to Combined oxidative phosphorylation deficiency 21, MIM# 615918
Mitochondrial disease v0.177 TARS2 Zornitza Stark Publications for gene: TARS2 were set to
Mitochondrial disease v0.176 TARS2 Zornitza Stark Mode of inheritance for gene: TARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.175 TARS2 Zornitza Stark Classified gene: TARS2 as Amber List (moderate evidence)
Mitochondrial disease v0.175 TARS2 Zornitza Stark Gene: tars2 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.174 TARS2 Zornitza Stark reviewed gene: TARS2: Rating: AMBER; Mode of pathogenicity: None; Publications: 24827421, 26811336; Phenotypes: Combined oxidative phosphorylation deficiency 21, MIM# 615918; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.174 STAT2 Zornitza Stark Marked gene: STAT2 as ready
Mitochondrial disease v0.174 STAT2 Zornitza Stark Gene: stat2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.174 STAT2 Zornitza Stark Phenotypes for gene: STAT2 were changed from to Immunodeficiency 44, MIM# 616636
Mitochondrial disease v0.173 STAT2 Zornitza Stark Publications for gene: STAT2 were set to
Mitochondrial disease v0.172 STAT2 Zornitza Stark Mode of inheritance for gene: STAT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.171 STAT2 Zornitza Stark reviewed gene: STAT2: Rating: GREEN; Mode of pathogenicity: None; Publications: 23391734, 26122121; Phenotypes: Immunodeficiency 44, MIM# 616636; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.171 SLC25A38 Zornitza Stark Marked gene: SLC25A38 as ready
Mitochondrial disease v0.171 SLC25A38 Zornitza Stark Gene: slc25a38 has been classified as Green List (High Evidence).
Mitochondrial disease v0.171 SLC25A38 Zornitza Stark Classified gene: SLC25A38 as Green List (high evidence)
Mitochondrial disease v0.171 SLC25A38 Zornitza Stark Gene: slc25a38 has been classified as Green List (High Evidence).
Mitochondrial disease v0.170 SLC25A38 Zornitza Stark gene: SLC25A38 was added
gene: SLC25A38 was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: SLC25A38 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC25A38 were set to 19412178
Phenotypes for gene: SLC25A38 were set to Anemia, sideroblastic, 2, pyridoxine-refractory, MIM# 205950
Review for gene: SLC25A38 was set to GREEN
Added comment: SLC25A38 belongs to the SLC25 family of mitochondrial carrier proteins. Multiple affected families reported together with an animal model.
Sources: Expert list
Mendeliome v0.1745 SLC25A32 Zornitza Stark Marked gene: SLC25A32 as ready
Mendeliome v0.1745 SLC25A32 Zornitza Stark Gene: slc25a32 has been classified as Green List (High Evidence).
Mendeliome v0.1745 SLC25A32 Zornitza Stark Classified gene: SLC25A32 as Green List (high evidence)
Mendeliome v0.1745 SLC25A32 Zornitza Stark Gene: slc25a32 has been classified as Green List (High Evidence).
Mendeliome v0.1744 SLC25A32 Zornitza Stark gene: SLC25A32 was added
gene: SLC25A32 was added to Mendeliome. Sources: Expert list
Mode of inheritance for gene: SLC25A32 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC25A32 were set to 26933868; 28443623
Phenotypes for gene: SLC25A32 were set to Exercise intolerance, riboflavin-responsive, MIM# 616839
Review for gene: SLC25A32 was set to GREEN
Added comment: Two unrelated families reported with functional data. Muscle biopsy showed ragged-red fibers and lipid storage mainly in type I oxidative fibers, small type II fibers, and poor immunostaining for succinate dehydrogenase (FAD-dependent mitochondrial respiratory chain complex II). Oral supplementation with riboflavin led to dramatic improvement in the clinical and biologic abnormalities.
Sources: Expert list
Mitochondrial disease v0.169 SLC25A32 Zornitza Stark Marked gene: SLC25A32 as ready
Mitochondrial disease v0.169 SLC25A32 Zornitza Stark Gene: slc25a32 has been classified as Green List (High Evidence).
Mitochondrial disease v0.169 SLC25A32 Zornitza Stark Classified gene: SLC25A32 as Green List (high evidence)
Mitochondrial disease v0.169 SLC25A32 Zornitza Stark Gene: slc25a32 has been classified as Green List (High Evidence).
Mitochondrial disease v0.168 SLC25A32 Zornitza Stark gene: SLC25A32 was added
gene: SLC25A32 was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: SLC25A32 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC25A32 were set to 26933868; 28443623
Phenotypes for gene: SLC25A32 were set to Exercise intolerance, riboflavin-responsive, MIM# 616839
Review for gene: SLC25A32 was set to GREEN
Added comment: Two unrelated families reported with functional data. Muscle biopsy showed ragged-red fibers and lipid storage mainly in type I oxidative fibers, small type II fibers, and poor immunostaining for succinate dehydrogenase (FAD-dependent mitochondrial respiratory chain complex II). Oral supplementation with riboflavin led to dramatic improvement in the clinical and biologic abnormalities.
Sources: Expert list
Mitochondrial disease v0.167 SDHB Zornitza Stark Marked gene: SDHB as ready
Mitochondrial disease v0.167 SDHB Zornitza Stark Gene: sdhb has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.167 SDHB Zornitza Stark Phenotypes for gene: SDHB were changed from to Complex II deficiency; mitochondrial leucoencephalopathy
Mitochondrial disease v0.166 SDHB Zornitza Stark Publications for gene: SDHB were set to
Mitochondrial disease v0.165 SDHB Zornitza Stark Mode of inheritance for gene: SDHB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.164 SDHB Zornitza Stark Classified gene: SDHB as Amber List (moderate evidence)
Mitochondrial disease v0.164 SDHB Zornitza Stark Gene: sdhb has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.163 SDHB Zornitza Stark reviewed gene: SDHB: Rating: AMBER; Mode of pathogenicity: None; Publications: 22972948, 26925370; Phenotypes: Complex II deficiency, mitochondrial leucoencephalopathy; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.163 SDHAF2 Zornitza Stark Marked gene: SDHAF2 as ready
Mitochondrial disease v0.163 SDHAF2 Zornitza Stark Gene: sdhaf2 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.163 SDHAF2 Zornitza Stark Phenotypes for gene: SDHAF2 were changed from to Paragangliomas 2, MIM# 601650
Mitochondrial disease v0.162 SDHAF2 Zornitza Stark Classified gene: SDHAF2 as Red List (low evidence)
Mitochondrial disease v0.162 SDHAF2 Zornitza Stark Gene: sdhaf2 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.161 SDHAF2 Zornitza Stark reviewed gene: SDHAF2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Paragangliomas 2, MIM# 601650; Mode of inheritance: None
Mitochondrial disease v0.161 SACS Zornitza Stark Marked gene: SACS as ready
Mitochondrial disease v0.161 SACS Zornitza Stark Gene: sacs has been classified as Green List (High Evidence).
Mitochondrial disease v0.161 SACS Zornitza Stark Classified gene: SACS as Green List (high evidence)
Mitochondrial disease v0.161 SACS Zornitza Stark Gene: sacs has been classified as Green List (High Evidence).
Mitochondrial disease v0.160 SACS Zornitza Stark gene: SACS was added
gene: SACS was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: SACS was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SACS were set to 22307627; 20876471
Phenotypes for gene: SACS were set to Spastic ataxia, Charlevoix-Saguenay type, MIM# 270550
Review for gene: SACS was set to GREEN
Added comment: Progressive neurological disorder, multiple families reported, mitochondrial dysfunction.
Sources: Expert list
Mitochondrial disease v0.159 PDK3 Zornitza Stark Marked gene: PDK3 as ready
Mitochondrial disease v0.159 PDK3 Zornitza Stark Gene: pdk3 has been classified as Green List (High Evidence).
Mitochondrial disease v0.159 PDK3 Zornitza Stark Phenotypes for gene: PDK3 were changed from to Charcot-Marie-Tooth disease, X-linked dominant, 6, MIM# 300905
Mitochondrial disease v0.158 PDK3 Zornitza Stark Publications for gene: PDK3 were set to
Mitochondrial disease v0.157 PDK3 Zornitza Stark Mode of inheritance for gene: PDK3 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Mitochondrial disease v0.156 PDK3 Zornitza Stark reviewed gene: PDK3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23297365, 28902413, 26801680; Phenotypes: Charcot-Marie-Tooth disease, X-linked dominant, 6, MIM# 300905; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Mitochondrial disease v0.156 PC Zornitza Stark Marked gene: PC as ready
Mitochondrial disease v0.156 PC Zornitza Stark Gene: pc has been classified as Green List (High Evidence).
Mitochondrial disease v0.156 PC Zornitza Stark Classified gene: PC as Green List (high evidence)
Mitochondrial disease v0.156 PC Zornitza Stark Gene: pc has been classified as Green List (High Evidence).
Mitochondrial disease v0.155 PC Zornitza Stark gene: PC was added
gene: PC was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: PC was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: PC were set to Pyruvate carboxylase deficiency, MIM# 266150
Review for gene: PC was set to GREEN
Added comment: Multiple families reported. Spectrum of severity ranging from death in infancy to a relatively benign condition. Correlates with variant impact with more severely affected individuals having at least one truncating variant.
Sources: Expert list
Mendeliome v0.1743 NFS1 Zornitza Stark Marked gene: NFS1 as ready
Mendeliome v0.1743 NFS1 Zornitza Stark Gene: nfs1 has been classified as Red List (Low Evidence).
Mendeliome v0.1743 NFS1 Zornitza Stark Phenotypes for gene: NFS1 were changed from to Complex II/III deficiency; multisystem organ failure
Mitochondrial disease v0.154 NFS1 Zornitza Stark Marked gene: NFS1 as ready
Mitochondrial disease v0.154 NFS1 Zornitza Stark Gene: nfs1 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.154 NFS1 Zornitza Stark Phenotypes for gene: NFS1 were changed from to Complex II/III deficiency; multisystem organ failure
Mendeliome v0.1742 NFS1 Zornitza Stark Publications for gene: NFS1 were set to
Mendeliome v0.1741 NFS1 Zornitza Stark Mode of inheritance for gene: NFS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1740 NFS1 Zornitza Stark Classified gene: NFS1 as Red List (low evidence)
Mendeliome v0.1740 NFS1 Zornitza Stark Gene: nfs1 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.153 NFS1 Zornitza Stark Publications for gene: NFS1 were set to
Mendeliome v0.1739 NFS1 Zornitza Stark reviewed gene: NFS1: Rating: RED; Mode of pathogenicity: None; Publications: 24498631; Phenotypes: Complex II/III deficiency, multisystem organ failure; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.152 NFS1 Zornitza Stark Mode of inheritance for gene: NFS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.151 NFS1 Zornitza Stark Classified gene: NFS1 as Red List (low evidence)
Mitochondrial disease v0.151 NFS1 Zornitza Stark Gene: nfs1 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.150 NFS1 Zornitza Stark reviewed gene: NFS1: Rating: RED; Mode of pathogenicity: None; Publications: 24498631; Phenotypes: Complex II/III deficiency, multisystem organ failure; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1739 NDUFA6 Zornitza Stark Marked gene: NDUFA6 as ready
Mendeliome v0.1739 NDUFA6 Zornitza Stark Gene: ndufa6 has been classified as Green List (High Evidence).
Mendeliome v0.1739 NDUFA6 Zornitza Stark Phenotypes for gene: NDUFA6 were changed from to Mitochondrial complex I deficiency, nuclear type 33, MIM# 618253
Mendeliome v0.1738 NDUFA6 Zornitza Stark Publications for gene: NDUFA6 were set to
Mendeliome v0.1737 NDUFA6 Zornitza Stark Mode of inheritance for gene: NDUFA6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1736 NDUFA6 Zornitza Stark reviewed gene: NDUFA6: Rating: GREEN; Mode of pathogenicity: None; Publications: 30245030; Phenotypes: Mitochondrial complex I deficiency, nuclear type 33, MIM# 618253; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.150 NDUFA6 Zornitza Stark Marked gene: NDUFA6 as ready
Mitochondrial disease v0.150 NDUFA6 Zornitza Stark Gene: ndufa6 has been classified as Green List (High Evidence).
Mitochondrial disease v0.150 NDUFA6 Zornitza Stark Classified gene: NDUFA6 as Green List (high evidence)
Mitochondrial disease v0.150 NDUFA6 Zornitza Stark Gene: ndufa6 has been classified as Green List (High Evidence).
Mitochondrial disease v0.149 NDUFA6 Zornitza Stark gene: NDUFA6 was added
gene: NDUFA6 was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: NDUFA6 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NDUFA6 were set to 30245030
Phenotypes for gene: NDUFA6 were set to Mitochondrial complex I deficiency, nuclear type 33, MIM# 618253
Review for gene: NDUFA6 was set to GREEN
gene: NDUFA6 was marked as current diagnostic
Added comment: Four unrelated children reported with bi-allelic variants in this gene and delayed development and/or neurologic deterioration in the first weeks or years of life. Two individuals died in infancy; the other 2 were unable to stand, walk, or speak, and had optic atrophy.
Sources: Expert list
Mitochondrial disease v0.148 NDUFA4 Zornitza Stark Marked gene: NDUFA4 as ready
Mitochondrial disease v0.148 NDUFA4 Zornitza Stark Gene: ndufa4 has been classified as Amber List (Moderate Evidence).
Regression v0.94 NDUFA4 Zornitza Stark Marked gene: NDUFA4 as ready
Regression v0.94 NDUFA4 Zornitza Stark Gene: ndufa4 has been classified as Red List (Low Evidence).
Regression v0.94 NDUFA4 Zornitza Stark Phenotypes for gene: NDUFA4 were changed from to Leigh syndrome; Complex IV deficiency
Regression v0.93 NDUFA4 Zornitza Stark Publications for gene: NDUFA4 were set to
Regression v0.92 NDUFA4 Zornitza Stark Classified gene: NDUFA4 as Red List (low evidence)
Regression v0.92 NDUFA4 Zornitza Stark Gene: ndufa4 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.148 NDUFA4 Zornitza Stark Phenotypes for gene: NDUFA4 were changed from to Leigh syndrome; Complex IV deficiency
Regression v0.91 NDUFA4 Zornitza Stark reviewed gene: NDUFA4: Rating: RED; Mode of pathogenicity: None; Publications: 30361421, 28988874, 23746447; Phenotypes: Leigh syndrome, Complex IV deficiency; Mode of inheritance: None
Mendeliome v0.1736 NDUFA4 Zornitza Stark Marked gene: NDUFA4 as ready
Mendeliome v0.1736 NDUFA4 Zornitza Stark Gene: ndufa4 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1736 NDUFA4 Zornitza Stark Phenotypes for gene: NDUFA4 were changed from to Leigh syndrome; Complex IV deficiency
Mendeliome v0.1735 NDUFA4 Zornitza Stark Publications for gene: NDUFA4 were set to
Mendeliome v0.1734 NDUFA4 Zornitza Stark Mode of inheritance for gene: NDUFA4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1733 NDUFA4 Zornitza Stark Classified gene: NDUFA4 as Amber List (moderate evidence)
Mendeliome v0.1733 NDUFA4 Zornitza Stark Gene: ndufa4 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1732 NDUFA4 Zornitza Stark reviewed gene: NDUFA4: Rating: AMBER; Mode of pathogenicity: None; Publications: 30361421, 28988874, 23746447; Phenotypes: Leigh syndrome, Complex IV deficiency; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.147 NDUFA4 Zornitza Stark Publications for gene: NDUFA4 were set to
Mitochondrial disease v0.146 NDUFA4 Zornitza Stark Mode of inheritance for gene: NDUFA4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.145 NDUFA4 Zornitza Stark Classified gene: NDUFA4 as Amber List (moderate evidence)
Mitochondrial disease v0.145 NDUFA4 Zornitza Stark Gene: ndufa4 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.144 NDUFA4 Zornitza Stark reviewed gene: NDUFA4: Rating: AMBER; Mode of pathogenicity: None; Publications: 30361421, 28988874, 23746447; Phenotypes: Leigh syndrome, Complex IV deficiency; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1732 NDUFA13 Zornitza Stark Marked gene: NDUFA13 as ready
Mendeliome v0.1732 NDUFA13 Zornitza Stark Gene: ndufa13 has been classified as Red List (Low Evidence).
Mendeliome v0.1732 NDUFA13 Zornitza Stark Phenotypes for gene: NDUFA13 were changed from to Mitochondrial complex I deficiency, nuclear type 28, MIM# 618249
Mendeliome v0.1731 NDUFA13 Zornitza Stark Publications for gene: NDUFA13 were set to
Mendeliome v0.1730 NDUFA13 Zornitza Stark Mode of inheritance for gene: NDUFA13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1729 NDUFA13 Zornitza Stark Classified gene: NDUFA13 as Red List (low evidence)
Mendeliome v0.1729 NDUFA13 Zornitza Stark Gene: ndufa13 has been classified as Red List (Low Evidence).
Mendeliome v0.1728 NDUFA13 Zornitza Stark reviewed gene: NDUFA13: Rating: RED; Mode of pathogenicity: None; Publications: 25901006; Phenotypes: Mitochondrial complex I deficiency, nuclear type 28, MIM# 618249; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.144 NDUFA13 Zornitza Stark Marked gene: NDUFA13 as ready
Mitochondrial disease v0.144 NDUFA13 Zornitza Stark Gene: ndufa13 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.144 NDUFA13 Zornitza Stark Phenotypes for gene: NDUFA13 were changed from to Mitochondrial complex I deficiency, nuclear type 28, MIM# 618249
Mitochondrial disease v0.143 NDUFA13 Zornitza Stark Publications for gene: NDUFA13 were set to
Mitochondrial disease v0.142 NDUFA13 Zornitza Stark Mode of inheritance for gene: NDUFA13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.141 NDUFA13 Zornitza Stark Classified gene: NDUFA13 as Red List (low evidence)
Mitochondrial disease v0.141 NDUFA13 Zornitza Stark Gene: ndufa13 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.140 NDUFA13 Zornitza Stark reviewed gene: NDUFA13: Rating: RED; Mode of pathogenicity: None; Publications: 25901006; Phenotypes: Mitochondrial complex I deficiency, nuclear type 28, MIM# 618249; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.140 NADK2 Zornitza Stark Marked gene: NADK2 as ready
Mitochondrial disease v0.140 NADK2 Zornitza Stark Gene: nadk2 has been classified as Green List (High Evidence).
Mendeliome v0.1728 NADK2 Zornitza Stark Marked gene: NADK2 as ready
Mendeliome v0.1728 NADK2 Zornitza Stark Gene: nadk2 has been classified as Green List (High Evidence).
Mendeliome v0.1728 NADK2 Zornitza Stark Classified gene: NADK2 as Green List (high evidence)
Mendeliome v0.1728 NADK2 Zornitza Stark Gene: nadk2 has been classified as Green List (High Evidence).
Mendeliome v0.1727 NADK2 Zornitza Stark gene: NADK2 was added
gene: NADK2 was added to Mendeliome. Sources: Expert list
Mode of inheritance for gene: NADK2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NADK2 were set to 24847004; 29388319; 27940755
Phenotypes for gene: NADK2 were set to 2,4-dienoyl-CoA reductase deficiency, MIM# 616034
Review for gene: NADK2 was set to GREEN
gene: NADK2 was marked as current diagnostic
Added comment: Mitochondrial dysfunction resulting in severe neurologic and metabolic dysfunction beginning in early infancy reported in two individuals with confirmed variants in this gene. Another individual with homozygous hypomorphic start loss variant g.36241900 A>G p. Met1Val and milder phenotype reported (PMID:29388319).
Sources: Expert list
Mitochondrial disease v0.140 NADK2 Zornitza Stark Classified gene: NADK2 as Green List (high evidence)
Mitochondrial disease v0.140 NADK2 Zornitza Stark Gene: nadk2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.139 NADK2 Zornitza Stark gene: NADK2 was added
gene: NADK2 was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: NADK2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NADK2 were set to 24847004; 29388319; 27940755
Phenotypes for gene: NADK2 were set to 2,4-dienoyl-CoA reductase deficiency, MIM# 616034
Review for gene: NADK2 was set to GREEN
Added comment: Mitochondrial dysfunction resulting in severe neurologic and metabolic dysfunction beginning in early infancy reported in two individuals with confirmed variants in this gene. Another individual with homozygous hypomorphic start loss variant g.36241900 A>G p. Met1Val and milder phenotype reported (PMID:29388319).
Sources: Expert list
Mitochondrial disease v0.138 MSTO1 Zornitza Stark Marked gene: MSTO1 as ready
Mitochondrial disease v0.138 MSTO1 Zornitza Stark Gene: msto1 has been classified as Green List (High Evidence).
Mitochondrial disease v0.138 MSTO1 Zornitza Stark Classified gene: MSTO1 as Green List (high evidence)
Mitochondrial disease v0.138 MSTO1 Zornitza Stark Gene: msto1 has been classified as Green List (High Evidence).
Mitochondrial disease v0.137 MSTO1 Zornitza Stark gene: MSTO1 was added
gene: MSTO1 was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: MSTO1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: MSTO1 were set to 28554942; 28544275; 31604776; 31463572; 31130378; 30684668; 29339779
Phenotypes for gene: MSTO1 were set to Myopathy, mitochondrial, and ataxia, MIM# 617675
Review for gene: MSTO1 was set to GREEN
gene: MSTO1 was marked as current diagnostic
Added comment: Impaired mitochondrial fusion disorder. Multiple families reported with bi-allelic variants and childhood-onset muscular dystrophy, corticospinal tract dysfunction and early-onset non-progressive cerebellar atrophy. One family reported with heterozygous variant in this gene, gene-disease association for mono allelic variants not well established.
Sources: Expert list
Genetic Epilepsy v0.635 ISCA1 Zornitza Stark Marked gene: ISCA1 as ready
Genetic Epilepsy v0.635 ISCA1 Zornitza Stark Gene: isca1 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.635 ISCA1 Zornitza Stark Classified gene: ISCA1 as Green List (high evidence)
Genetic Epilepsy v0.635 ISCA1 Zornitza Stark Gene: isca1 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.634 ISCA1 Zornitza Stark gene: ISCA1 was added
gene: ISCA1 was added to Genetic Epilepsy. Sources: Expert list
Mode of inheritance for gene: ISCA1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ISCA1 were set to 28356563; 32092383; 31016283; 30113620; 30105122
Phenotypes for gene: ISCA1 were set to Multiple mitochondrial dysfunctions syndrome 5, MIM# 617613
Review for gene: ISCA1 was set to GREEN
Added comment: Multiple unrelated families reported. Severe disorder characterised by progressive neurologic deterioration beginning in early infancy. Affected individuals have essentially no psychomotor development and have early-onset seizures with neurologic decline and spasticity. Brain imaging shows severe leukodystrophy with evidence of dys- or delayed myelination. Rat model results in early lethality. Founder variant c.259G > A, p.(Glu87Lys) reported in Indian families.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2470 ISCA1 Zornitza Stark Marked gene: ISCA1 as ready
Intellectual disability syndromic and non-syndromic v0.2470 ISCA1 Zornitza Stark Gene: isca1 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2470 ISCA1 Zornitza Stark Classified gene: ISCA1 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2470 ISCA1 Zornitza Stark Gene: isca1 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2469 ISCA1 Zornitza Stark gene: ISCA1 was added
gene: ISCA1 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: ISCA1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ISCA1 were set to 28356563; 32092383; 31016283; 30113620; 30105122
Phenotypes for gene: ISCA1 were set to Multiple mitochondrial dysfunctions syndrome 5, MIM# 617613
Review for gene: ISCA1 was set to GREEN
gene: ISCA1 was marked as current diagnostic
Added comment: Multiple unrelated families reported. Severe disorder characterised by progressive neurologic deterioration beginning in early infancy. Affected individuals have essentially no psychomotor development and have early-onset seizures with neurologic decline and spasticity. Brain imaging shows severe leukodystrophy with evidence of dys- or delayed myelination. Rat model results in early lethality. Founder variant c.259G > A, p.(Glu87Lys) reported in Indian families.
Sources: Expert list
Regression v0.91 ISCA1 Zornitza Stark Marked gene: ISCA1 as ready
Regression v0.91 ISCA1 Zornitza Stark Gene: isca1 has been classified as Green List (High Evidence).
Regression v0.91 ISCA1 Zornitza Stark Classified gene: ISCA1 as Green List (high evidence)
Regression v0.91 ISCA1 Zornitza Stark Gene: isca1 has been classified as Green List (High Evidence).
Regression v0.90 ISCA1 Zornitza Stark gene: ISCA1 was added
gene: ISCA1 was added to Regression. Sources: Expert list
Mode of inheritance for gene: ISCA1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ISCA1 were set to 28356563; 32092383; 31016283; 30113620; 30105122
Phenotypes for gene: ISCA1 were set to Multiple mitochondrial dysfunctions syndrome 5, MIM# 617613
Review for gene: ISCA1 was set to GREEN
gene: ISCA1 was marked as current diagnostic
Added comment: Multiple unrelated families reported. Severe disorder characterised by progressive neurologic deterioration beginning in early infancy. Affected individuals have essentially no psychomotor development and have early-onset seizures with neurologic decline and spasticity. Brain imaging shows severe leukodystrophy with evidence of dys- or delayed myelination. Rat model results in early lethality. Founder variant c.259G > A, p.(Glu87Lys) reported in Indian families.
Sources: Expert list
Mendeliome v0.1726 ISCA1 Zornitza Stark Marked gene: ISCA1 as ready
Mendeliome v0.1726 ISCA1 Zornitza Stark Gene: isca1 has been classified as Green List (High Evidence).
Mendeliome v0.1726 ISCA1 Zornitza Stark Classified gene: ISCA1 as Green List (high evidence)
Mendeliome v0.1726 ISCA1 Zornitza Stark Gene: isca1 has been classified as Green List (High Evidence).
Mendeliome v0.1725 ISCA1 Zornitza Stark gene: ISCA1 was added
gene: ISCA1 was added to Mendeliome. Sources: Expert list
Mode of inheritance for gene: ISCA1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ISCA1 were set to 28356563; 32092383; 31016283; 30113620; 30105122
Phenotypes for gene: ISCA1 were set to Multiple mitochondrial dysfunctions syndrome 5, MIM# 617613
Review for gene: ISCA1 was set to GREEN
gene: ISCA1 was marked as current diagnostic
Added comment: Multiple unrelated families reported. Severe disorder characterised by progressive neurologic deterioration beginning in early infancy. Affected individuals have essentially no psychomotor development and have early-onset seizures with neurologic decline and spasticity. Brain imaging shows severe leukodystrophy with evidence of dys- or delayed myelination. Rat model results in early lethality. Founder variant c.259G > A, p.(Glu87Lys) reported in Indian families.
Sources: Expert list
Mitochondrial disease v0.136 ISCA1 Zornitza Stark Marked gene: ISCA1 as ready
Mitochondrial disease v0.136 ISCA1 Zornitza Stark Gene: isca1 has been classified as Green List (High Evidence).
Mitochondrial disease v0.136 ISCA1 Zornitza Stark Classified gene: ISCA1 as Green List (high evidence)
Mitochondrial disease v0.136 ISCA1 Zornitza Stark Gene: isca1 has been classified as Green List (High Evidence).
Mitochondrial disease v0.135 ISCA1 Zornitza Stark gene: ISCA1 was added
gene: ISCA1 was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: ISCA1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ISCA1 were set to 28356563; 32092383; 31016283; 30113620; 30105122
Phenotypes for gene: ISCA1 were set to Multiple mitochondrial dysfunctions syndrome 5, MIM# 617613
Review for gene: ISCA1 was set to GREEN
gene: ISCA1 was marked as current diagnostic
Added comment: Multiple unrelated families reported. Severe disorder characterised by progressive neurologic deterioration beginning in early infancy. Affected individuals have essentially no psychomotor development and have early-onset seizures with neurologic decline and spasticity. Brain imaging shows severe leukodystrophy with evidence of dys- or delayed myelination. Rat model results in early lethality. Founder variant c.259G > A, p.(Glu87Lys) reported in Indian families.
Sources: Expert list
Mitochondrial disease v0.134 IDH3B Zornitza Stark Marked gene: IDH3B as ready
Mitochondrial disease v0.134 IDH3B Zornitza Stark Gene: idh3b has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.134 IDH3B Zornitza Stark Phenotypes for gene: IDH3B were changed from to Retinitis pigmentosa 46, MIM# 612572
Mitochondrial disease v0.133 IDH3B Zornitza Stark Publications for gene: IDH3B were set to
Mitochondrial disease v0.132 IDH3B Zornitza Stark Mode of inheritance for gene: IDH3B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.131 IDH3B Zornitza Stark Classified gene: IDH3B as Amber List (moderate evidence)
Mitochondrial disease v0.131 IDH3B Zornitza Stark Gene: idh3b has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.130 IDH3B Zornitza Stark reviewed gene: IDH3B: Rating: AMBER; Mode of pathogenicity: None; Publications: 18806796, 31736247; Phenotypes: Retinitis pigmentosa 46, MIM# 612572; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.130 HTRA2 Zornitza Stark Marked gene: HTRA2 as ready
Mitochondrial disease v0.130 HTRA2 Zornitza Stark Gene: htra2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.130 HTRA2 Zornitza Stark Classified gene: HTRA2 as Green List (high evidence)
Mitochondrial disease v0.130 HTRA2 Zornitza Stark Gene: htra2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.129 HTRA2 Zornitza Stark gene: HTRA2 was added
gene: HTRA2 was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: HTRA2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: HTRA2 were set to 27208207; 27696117
Phenotypes for gene: HTRA2 were set to 3-methylglutaconic aciduria, type VIII, MIM# 617248
Review for gene: HTRA2 was set to GREEN
gene: HTRA2 was marked as current diagnostic
Added comment: Severe disorder typically presenting with hypotonia, abnormal movements, respiratory insufficiency with apnoea, and lack of developmental progress, often with seizures. Brain imaging is variable, but may show progressive cerebral atrophy. Increased serum lactate and 3-methylglutaconic aciduria. At least four unrelated families reported.
Sources: Expert list
Mendeliome v0.1724 ERCC5 Zornitza Stark Marked gene: ERCC5 as ready
Mendeliome v0.1724 ERCC5 Zornitza Stark Gene: ercc5 has been classified as Green List (High Evidence).
Mendeliome v0.1724 ERCC5 Zornitza Stark Phenotypes for gene: ERCC5 were changed from to Cerebrooculofacioskeletal syndrome 3, MIM# 616570; Xeroderma pigmentosum, group G, MIM# 278780; Xeroderma pigmentosum, group G/Cockayne syndrome, MIM# 278780
Mendeliome v0.1723 ERCC5 Zornitza Stark Publications for gene: ERCC5 were set to
Mendeliome v0.1722 ERCC5 Zornitza Stark Mode of inheritance for gene: ERCC5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1721 BTD Zornitza Stark Marked gene: BTD as ready
Mendeliome v0.1721 BTD Zornitza Stark Gene: btd has been classified as Green List (High Evidence).
Mendeliome v0.1721 BTD Zornitza Stark Phenotypes for gene: BTD were changed from to Biotinidase deficiency, MIM 253260
Mendeliome v0.1720 BTD Zornitza Stark Publications for gene: BTD were set to
Mendeliome v0.1719 BTD Zornitza Stark Mode of inheritance for gene: BTD was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1718 CTNNB1 Zornitza Stark Marked gene: CTNNB1 as ready
Mendeliome v0.1718 CTNNB1 Zornitza Stark Gene: ctnnb1 has been classified as Green List (High Evidence).
Mendeliome v0.1718 CTNNB1 Zornitza Stark Phenotypes for gene: CTNNB1 were changed from to Exudative vitreoretinopathy 7, MIM# 617572; Neurodevelopmental disorder with spastic diplegia and visual defects, MIM# 615075
Mendeliome v0.1717 CTNNB1 Zornitza Stark Publications for gene: CTNNB1 were set to
Mendeliome v0.1716 CTNNB1 Zornitza Stark Mode of pathogenicity for gene: CTNNB1 was changed from to Other
Mendeliome v0.1715 CTNNB1 Zornitza Stark Mode of inheritance for gene: CTNNB1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1714 CTNNB1 Zornitza Stark reviewed gene: CTNNB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25326669, 29435196, 27915094, 30640974; Phenotypes: Exudative vitreoretinopathy 7, MIM# 617572, Neurodevelopmental disorder with spastic diplegia and visual defects, MIM# 615075; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1714 ERCC5 Chern Lim reviewed gene: ERCC5: Rating: GREEN; Mode of pathogenicity: None; Publications: 30838033, 24700531; Phenotypes: Cerebrooculofacioskeletal syndrome 3, MIM# 616570, Xeroderma pigmentosum, group G, MIM# 278780, Xeroderma pigmentosum, group G/Cockayne syndrome, MIM# 278780; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1714 BTD Chern Lim reviewed gene: BTD: Rating: GREEN; Mode of pathogenicity: None; Publications: 10801053, 12359137; Phenotypes: Biotinidase deficiency, MIM 253260; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1714 CTNNB1 Teresa Zhao changed review comment from: OMIM:
LoF - mainly non cancerous phenotypes, and
GoF - mainly cancer phenotypes.

Cancer hot spot in exon 3, mainly missenses affecting S33, S37, S45, T41, D32 and G34 (Gao. C. et al. 2017); to: OMIM:
LoF - mainly non cancerous phenotypes, and
GoF - mainly cancer phenotypes.

Cancer hot spot in exon 3, mainly missenses affecting S33, S37, S45, T41, D32 and G34 (Gao. C. et al. 2017)
Mendeliome v0.1714 CTNNB1 Teresa Zhao reviewed gene: CTNNB1: Rating: GREEN; Mode of pathogenicity: Other; Publications: ; Phenotypes: PMID: 29435196, PMID: 27915094, PMID: 30640974; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Proteinuria v0.106 KANK4 Zornitza Stark edited their review of gene: KANK4: Changed phenotypes: Nephrotic syndrome
Mendeliome v0.1714 KANK4 Zornitza Stark edited their review of gene: KANK4: Changed rating: RED
Mendeliome v0.1714 TET2 Zornitza Stark Marked gene: TET2 as ready
Mendeliome v0.1714 TET2 Zornitza Stark Gene: tet2 has been classified as Red List (Low Evidence).
Mendeliome v0.1714 TET2 Zornitza Stark Classified gene: TET2 as Red List (low evidence)
Mendeliome v0.1714 TET2 Zornitza Stark Gene: tet2 has been classified as Red List (Low Evidence).
Mendeliome v0.1713 TET2 Zornitza Stark reviewed gene: TET2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic v0.71 TRAP1 Zornitza Stark Marked gene: TRAP1 as ready
Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic v0.71 TRAP1 Zornitza Stark Gene: trap1 has been classified as Green List (High Evidence).
Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic v0.71 TRAP1 Zornitza Stark Phenotypes for gene: TRAP1 were changed from to CAKUT; VACTERL
Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic v0.70 TRAP1 Zornitza Stark Publications for gene: TRAP1 were set to
Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic v0.69 TRAP1 Zornitza Stark Mode of inheritance for gene: TRAP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic v0.68 TRAP1 Zornitza Stark reviewed gene: TRAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 24152966; Phenotypes: CAKUT, VACTERL; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1713 ARL11 Zornitza Stark Marked gene: ARL11 as ready
Mendeliome v0.1713 ARL11 Zornitza Stark Gene: arl11 has been classified as Red List (Low Evidence).
Mendeliome v0.1713 ARL11 Zornitza Stark Mode of inheritance for gene: ARL11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1712 ARL11 Zornitza Stark Classified gene: ARL11 as Red List (low evidence)
Mendeliome v0.1712 ARL11 Zornitza Stark Gene: arl11 has been classified as Red List (Low Evidence).
Mendeliome v0.1711 ARL11 Zornitza Stark reviewed gene: ARL11: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1711 CLCN6 Zornitza Stark Marked gene: CLCN6 as ready
Mendeliome v0.1711 CLCN6 Zornitza Stark Gene: clcn6 has been classified as Red List (Low Evidence).
Mendeliome v0.1711 CLCN6 Zornitza Stark Phenotypes for gene: CLCN6 were changed from to Benign partial epilepsy; febrile seizures; NCL
Mendeliome v0.1710 CLCN6 Zornitza Stark Publications for gene: CLCN6 were set to
Mendeliome v0.1709 CLCN6 Zornitza Stark Mode of inheritance for gene: CLCN6 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mendeliome v0.1708 CLCN6 Zornitza Stark Classified gene: CLCN6 as Red List (low evidence)
Mendeliome v0.1708 CLCN6 Zornitza Stark Gene: clcn6 has been classified as Red List (Low Evidence).
Mendeliome v0.1707 CLCN6 Zornitza Stark reviewed gene: CLCN6: Rating: RED; Mode of pathogenicity: None; Publications: 25794116, 21107136; Phenotypes: Benign partial epilepsy, febrile seizures, NCL; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Lysosomal Storage Disorder v0.5 CLCN6 Zornitza Stark Marked gene: CLCN6 as ready
Lysosomal Storage Disorder v0.5 CLCN6 Zornitza Stark Gene: clcn6 has been classified as Red List (Low Evidence).
Lysosomal Storage Disorder v0.5 CLCN6 Zornitza Stark Phenotypes for gene: CLCN6 were changed from to Benign partial epilepsy; febrile seizures; NCL
Lysosomal Storage Disorder v0.4 CLCN6 Zornitza Stark Publications for gene: CLCN6 were set to
Lysosomal Storage Disorder v0.3 CLCN6 Zornitza Stark Mode of inheritance for gene: CLCN6 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Lysosomal Storage Disorder v0.2 CLCN6 Zornitza Stark Classified gene: CLCN6 as Red List (low evidence)
Lysosomal Storage Disorder v0.2 CLCN6 Zornitza Stark Gene: clcn6 has been classified as Red List (Low Evidence).
Lysosomal Storage Disorder v0.1 CLCN6 Zornitza Stark edited their review of gene: CLCN6: Changed phenotypes: Benign partial epilepsy, febrile seizures, NCL; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Lysosomal Storage Disorder v0.1 CLCN6 Zornitza Stark reviewed gene: CLCN6: Rating: RED; Mode of pathogenicity: None; Publications: 25794116, 21107136; Phenotypes: Benign partial epilepsy, febrile seizures; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1707 SEMA6B Zornitza Stark Marked gene: SEMA6B as ready
Mendeliome v0.1707 SEMA6B Zornitza Stark Gene: sema6b has been classified as Green List (High Evidence).
Mendeliome v0.1707 SEMA6B Zornitza Stark Classified gene: SEMA6B as Green List (high evidence)
Mendeliome v0.1707 SEMA6B Zornitza Stark Gene: sema6b has been classified as Green List (High Evidence).
Mendeliome v0.1706 SEMA6B Zornitza Stark gene: SEMA6B was added
gene: SEMA6B was added to Mendeliome. Sources: Literature
Mode of inheritance for gene: SEMA6B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SEMA6B were set to 32169168
Phenotypes for gene: SEMA6B were set to Progressive myoclonic epilepsy
Mode of pathogenicity for gene: SEMA6B was set to Other
Review for gene: SEMA6B was set to GREEN
Added comment: Five individuals from unrelated families reported with de novo variants in the last exon, escaping NMD.
Sources: Literature
Genetic Epilepsy v0.633 SEMA6B Zornitza Stark Marked gene: SEMA6B as ready
Genetic Epilepsy v0.633 SEMA6B Zornitza Stark Gene: sema6b has been classified as Green List (High Evidence).
Genetic Epilepsy v0.633 SEMA6B Zornitza Stark Classified gene: SEMA6B as Green List (high evidence)
Genetic Epilepsy v0.633 SEMA6B Zornitza Stark Gene: sema6b has been classified as Green List (High Evidence).
Genetic Epilepsy v0.632 SEMA6B Zornitza Stark gene: SEMA6B was added
gene: SEMA6B was added to Genetic Epilepsy. Sources: Literature
Mode of inheritance for gene: SEMA6B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SEMA6B were set to 32169168
Phenotypes for gene: SEMA6B were set to Progressive myoclonic epilepsy
Mode of pathogenicity for gene: SEMA6B was set to Other
Review for gene: SEMA6B was set to GREEN
Added comment: Five individuals from unrelated families reported with de novo variants in the last exon, escaping NMD.
Sources: Literature
Mendeliome v0.1705 IFT74 Zornitza Stark Publications for gene: IFT74 were set to 27486776
Mendeliome v0.1704 IFT74 Zornitza Stark Classified gene: IFT74 as Green List (high evidence)
Mendeliome v0.1704 IFT74 Zornitza Stark Gene: ift74 has been classified as Green List (High Evidence).
Mendeliome v0.1703 IFT74 Zornitza Stark edited their review of gene: IFT74: Added comment: Second individual with bi-allelic variants and BBS phenotype reported.; Changed rating: GREEN; Changed publications: 27486776, 32144365
Ciliopathies v0.73 IFT74 Zornitza Stark Classified gene: IFT74 as Green List (high evidence)
Ciliopathies v0.73 IFT74 Zornitza Stark Gene: ift74 has been classified as Green List (High Evidence).
Ciliopathies v0.72 IFT74 Zornitza Stark edited their review of gene: IFT74: Added comment: Second individual with bi-allelic variants reported.; Changed rating: GREEN; Changed publications: 27486776, 32144365
Bardet Biedl syndrome v0.23 IFT74 Zornitza Stark Publications for gene: IFT74 were set to 27486776
Bardet Biedl syndrome v0.22 IFT74 Zornitza Stark Classified gene: IFT74 as Green List (high evidence)
Bardet Biedl syndrome v0.22 IFT74 Zornitza Stark Gene: ift74 has been classified as Green List (High Evidence).
Bardet Biedl syndrome v0.21 IFT74 Zornitza Stark edited their review of gene: IFT74: Changed rating: GREEN
Bardet Biedl syndrome v0.21 IFT74 Zornitza Stark changed review comment from: Single family plus functional data.
Sources: Expert list; to: Single family plus functional data (zebrafish model consistent with ciliopathy).
Sources: Expert list
Bardet Biedl syndrome v0.21 IFT74 Zornitza Stark edited their review of gene: IFT74: Added comment: Second individual with bi-allelic variants reported.; Changed publications: 27486776, 32144365
Renal Ciliopathies and Nephronophthisis v0.99 IFT74 Zornitza Stark Publications for gene: IFT74 were set to 27486776
Renal Ciliopathies and Nephronophthisis v0.98 IFT74 Zornitza Stark edited their review of gene: IFT74: Added comment: Second individual with bi-allelic variants reported. However, neither had renal disease.; Changed publications: 27486776, 32144365
Mendeliome v0.1703 CAMTA1 Zornitza Stark Marked gene: CAMTA1 as ready
Mendeliome v0.1703 CAMTA1 Zornitza Stark Gene: camta1 has been classified as Green List (High Evidence).
Mendeliome v0.1703 CAMTA1 Zornitza Stark Phenotypes for gene: CAMTA1 were changed from to Cerebellar ataxia, nonprogressive, with mental retardation (614756 AD)
Mendeliome v0.1702 CAMTA1 Zornitza Stark Publications for gene: CAMTA1 were set to
Mendeliome v0.1701 CAMTA1 Zornitza Stark Mode of inheritance for gene: CAMTA1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1700 CAMTA1 Zornitza Stark Tag SV/CNV tag was added to gene: CAMTA1.
Mendeliome v0.1700 CAMTA1 Zornitza Stark reviewed gene: CAMTA1: Rating: GREEN; Mode of pathogenicity: None; Publications: 32157189, 22693284; Phenotypes: Cerebellar ataxia, nonprogressive, with mental retardation (614756 AD); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Regression v0.89 CAMTA1 Zornitza Stark Marked gene: CAMTA1 as ready
Regression v0.89 CAMTA1 Zornitza Stark Gene: camta1 has been classified as Red List (Low Evidence).
Regression v0.89 CAMTA1 Zornitza Stark Phenotypes for gene: CAMTA1 were changed from to Cerebellar ataxia, nonprogressive, with mental retardation (614756 AD)
Regression v0.88 CAMTA1 Zornitza Stark Publications for gene: CAMTA1 were set to
Regression v0.87 CAMTA1 Zornitza Stark Mode of inheritance for gene: CAMTA1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Regression v0.86 CAMTA1 Zornitza Stark Classified gene: CAMTA1 as Red List (low evidence)
Regression v0.86 CAMTA1 Zornitza Stark Gene: camta1 has been classified as Red List (Low Evidence).
Regression v0.85 CAMTA1 Zornitza Stark reviewed gene: CAMTA1: Rating: RED; Mode of pathogenicity: None; Publications: 32157189, 22693284; Phenotypes: Cerebellar ataxia, nonprogressive, with mental retardation (614756 AD); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2468 CAMTA1 Zornitza Stark Publications for gene: CAMTA1 were set to
Intellectual disability syndromic and non-syndromic v0.2467 CAMTA1 Zornitza Stark Tag SV/CNV tag was added to gene: CAMTA1.
Intellectual disability syndromic and non-syndromic v0.2467 CAMTA1 Zornitza Stark reviewed gene: CAMTA1: Rating: GREEN; Mode of pathogenicity: None; Publications: 32157189, 22693284; Phenotypes: Cerebellar ataxia, nonprogressive, with mental retardation (614756 AD); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1700 TNNI3K Zornitza Stark Marked gene: TNNI3K as ready
Mendeliome v0.1700 TNNI3K Zornitza Stark Gene: tnni3k has been classified as Green List (High Evidence).
Mendeliome v0.1700 TNNI3K Zornitza Stark Classified gene: TNNI3K as Green List (high evidence)
Mendeliome v0.1700 TNNI3K Zornitza Stark Gene: tnni3k has been classified as Green List (High Evidence).
Mendeliome v0.1699 TNNI3K Zornitza Stark gene: TNNI3K was added
gene: TNNI3K was added to Mendeliome. Sources: Expert list
Mode of inheritance for gene: TNNI3K was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: TNNI3K were set to 30010057; 29355681
Phenotypes for gene: TNNI3K were set to Cardiac conduction disease with or without dilated cardiomyopathy, MIM# 616117
Review for gene: TNNI3K was set to GREEN
gene: TNNI3K was marked as current diagnostic
Added comment: At least 6 multigenerational families reported where variants segregated with disease.
Sources: Expert list
Dilated Cardiomyopathy v0.22 TNNI3K Zornitza Stark Marked gene: TNNI3K as ready
Dilated Cardiomyopathy v0.22 TNNI3K Zornitza Stark Added comment: Comment when marking as ready: At least 6 multigenerational families reported where variants segregated with disease.
Dilated Cardiomyopathy v0.22 TNNI3K Zornitza Stark Gene: tnni3k has been classified as Green List (High Evidence).
Dilated Cardiomyopathy v0.22 TNNI3K Zornitza Stark Phenotypes for gene: TNNI3K were changed from Cardiac conduction disease with or without dilated cardiomyopathy 616117 to Cardiac conduction disease with or without dilated cardiomyopathy, MIM# 616117
Dilated Cardiomyopathy v0.21 TNNI3K Zornitza Stark Classified gene: TNNI3K as Green List (high evidence)
Dilated Cardiomyopathy v0.21 TNNI3K Zornitza Stark Gene: tnni3k has been classified as Green List (High Evidence).
Dilated Cardiomyopathy v0.20 TNNI3K Ivan Macciocca gene: TNNI3K was added
gene: TNNI3K was added to Dilated Cardiomyopathy. Sources: Expert list
Mode of inheritance for gene: TNNI3K was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: TNNI3K were set to 30010057; 29355681
Phenotypes for gene: TNNI3K were set to Cardiac conduction disease with or without dilated cardiomyopathy 616117
Review for gene: TNNI3K was set to GREEN
gene: TNNI3K was marked as current diagnostic
Added comment: mutliple families reported. Green on England PanelApp
Sources: Expert list
Ectodermal Dysplasia v0.21 KREMEN1 Zornitza Stark Marked gene: KREMEN1 as ready
Ectodermal Dysplasia v0.21 KREMEN1 Zornitza Stark Gene: kremen1 has been classified as Amber List (Moderate Evidence).
Ectodermal Dysplasia v0.21 KREMEN1 Zornitza Stark Publications for gene: KREMEN1 were set to
Ectodermal Dysplasia v0.20 KREMEN1 Zornitza Stark Classified gene: KREMEN1 as Amber List (moderate evidence)
Ectodermal Dysplasia v0.20 KREMEN1 Zornitza Stark Gene: kremen1 has been classified as Amber List (Moderate Evidence).
Ectodermal Dysplasia v0.19 KREMEN1 Zornitza Stark reviewed gene: KREMEN1: Rating: AMBER; Mode of pathogenicity: None; Publications: 29526031, 29526031; Phenotypes: Ectodermal dysplasia 13, hair/tooth type, 617392; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ectodermal Dysplasia v0.19 Zornitza Stark Panel name changed from Ectodermal Dysplasia_RMH to Ectodermal Dysplasia
Panel types changed to Victorian Clinical Genetics Services; Royal Melbourne Hospital; Rare Disease
Ectodermal Dysplasia v0.18 ENAM Zornitza Stark Marked gene: ENAM as ready
Ectodermal Dysplasia v0.18 ENAM Zornitza Stark Gene: enam has been classified as Red List (Low Evidence).
Ectodermal Dysplasia v0.18 ENAM Zornitza Stark gene: ENAM was added
gene: ENAM was added to Ectodermal Dysplasia_RMH. Sources: Expert list
Mode of inheritance for gene: ENAM was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes for gene: ENAM were set to Amelogenesis imperfecta, type IB, MIM# 104500; Amelogenesis imperfecta, type IC, MIM# 204650
Review for gene: ENAM was set to RED
Added comment: Affects teeth only.
Sources: Expert list
Ectodermal Dysplasia v0.17 PKP1 Bryony Thompson Marked gene: PKP1 as ready
Ectodermal Dysplasia v0.17 PKP1 Bryony Thompson Gene: pkp1 has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.17 PKP1 Bryony Thompson Classified gene: PKP1 as Green List (high evidence)
Ectodermal Dysplasia v0.17 PKP1 Bryony Thompson Gene: pkp1 has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.16 PKP1 Bryony Thompson gene: PKP1 was added
gene: PKP1 was added to Ectodermal Dysplasia_RMH. Sources: Expert list
Mode of inheritance for gene: PKP1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PKP1 were set to 26288439; 9326952
Phenotypes for gene: PKP1 were set to Ectodermal dysplasia/skin fragility syndrome MIM#604536
Review for gene: PKP1 was set to GREEN
Added comment: Ectodermal dysplasia is a prominent feature of the condition. >3 cases reported.
Sources: Expert list
Microcephaly v0.100 GPT2 Zornitza Stark Marked gene: GPT2 as ready
Microcephaly v0.100 GPT2 Zornitza Stark Gene: gpt2 has been classified as Green List (High Evidence).
Microcephaly v0.100 GPT2 Zornitza Stark Classified gene: GPT2 as Green List (high evidence)
Microcephaly v0.100 GPT2 Zornitza Stark Gene: gpt2 has been classified as Green List (High Evidence).
Microcephaly v0.99 GPT2 Zornitza Stark gene: GPT2 was added
gene: GPT2 was added to Microcephaly. Sources: Expert list
Mode of inheritance for gene: GPT2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GPT2 were set to 27601654; 25758935
Phenotypes for gene: GPT2 were set to Mental retardation, autosomal recessive 49, MIM#616281
Review for gene: GPT2 was set to GREEN
Added comment: Two missense and 1 truncating variants reported, in 3 unrelated consanguineous families with intellectual and developmental disabilities and microcephaly. Functional studies showed loss of enzyme activity.
Sources: Expert list
Ectodermal Dysplasia v0.15 NFKBIA Bryony Thompson Marked gene: NFKBIA as ready
Ectodermal Dysplasia v0.15 NFKBIA Bryony Thompson Gene: nfkbia has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.15 NFKBIA Bryony Thompson Classified gene: NFKBIA as Green List (high evidence)
Ectodermal Dysplasia v0.15 NFKBIA Bryony Thompson Gene: nfkbia has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.14 NFKBIA Bryony Thompson gene: NFKBIA was added
gene: NFKBIA was added to Ectodermal Dysplasia_RMH. Sources: Expert list
Mode of inheritance for gene: NFKBIA was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: NFKBIA were set to 28597146
Phenotypes for gene: NFKBIA were set to Ectodermal dysplasia and immunodeficiency 2 MIM#612132
Mode of pathogenicity for gene: NFKBIA was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Review for gene: NFKBIA was set to GREEN
Added comment: Ectodermal dysplasia is a feature of the condition. >3 cases reported. Gain-of-function missense variants and nonsense variants upstream from S32 associated with the reinitiation of translation downstream.
Sources: Expert list
Mendeliome v0.1698 GPT2 Zornitza Stark Marked gene: GPT2 as ready
Mendeliome v0.1698 GPT2 Zornitza Stark Gene: gpt2 has been classified as Green List (High Evidence).
Mendeliome v0.1698 GPT2 Zornitza Stark Phenotypes for gene: GPT2 were changed from to Mental retardation, autosomal recessive 49, MIM#616281
Mendeliome v0.1697 GPT2 Zornitza Stark Publications for gene: GPT2 were set to
Mendeliome v0.1696 GPT2 Zornitza Stark Mode of inheritance for gene: GPT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1695 GPT2 Zornitza Stark reviewed gene: GPT2: Rating: GREEN; Mode of pathogenicity: None; Publications: 27601654, 25758935; Phenotypes: Mental retardation, autosomal recessive 49, MIM#616281; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2467 GPT2 Zornitza Stark Marked gene: GPT2 as ready
Intellectual disability syndromic and non-syndromic v0.2467 GPT2 Zornitza Stark Gene: gpt2 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2467 GPT2 Zornitza Stark Phenotypes for gene: GPT2 were changed from to Mental retardation, autosomal recessive 49, MIM#616281
Intellectual disability syndromic and non-syndromic v0.2466 GPT2 Zornitza Stark Publications for gene: GPT2 were set to
Intellectual disability syndromic and non-syndromic v0.2465 GPT2 Zornitza Stark Mode of inheritance for gene: GPT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Ectodermal Dysplasia v0.13 NECTIN1 Bryony Thompson Marked gene: NECTIN1 as ready
Ectodermal Dysplasia v0.13 NECTIN1 Bryony Thompson Gene: nectin1 has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.13 NECTIN1 Bryony Thompson Classified gene: NECTIN1 as Green List (high evidence)
Ectodermal Dysplasia v0.13 NECTIN1 Bryony Thompson Gene: nectin1 has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.12 NECTIN1 Bryony Thompson gene: NECTIN1 was added
gene: NECTIN1 was added to Ectodermal Dysplasia_RMH. Sources: Expert list
Mode of inheritance for gene: NECTIN1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NECTIN1 were set to 25913853
Phenotypes for gene: NECTIN1 were set to Cleft lip/palate-ectodermal dysplasia syndrome MIM#225060
Review for gene: NECTIN1 was set to GREEN
Added comment: Ectodermal dysplasia is a feature of the condition. >3 cases reported
Sources: Expert list
Ectodermal Dysplasia v0.11 KRT74 Bryony Thompson Classified gene: KRT74 as Amber List (moderate evidence)
Ectodermal Dysplasia v0.11 KRT74 Bryony Thompson Gene: krt74 has been classified as Amber List (Moderate Evidence).
Ectodermal Dysplasia v0.10 KRT74 Bryony Thompson reviewed gene: KRT74: Rating: AMBER; Mode of pathogenicity: None; Publications: 24714551; Phenotypes: Ectodermal dysplasia 7, hair/nail type MIM#614929; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ectodermal Dysplasia v0.10 IKBKG Bryony Thompson Marked gene: IKBKG as ready
Ectodermal Dysplasia v0.10 IKBKG Bryony Thompson Gene: ikbkg has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.10 IKBKG Bryony Thompson Classified gene: IKBKG as Green List (high evidence)
Ectodermal Dysplasia v0.10 IKBKG Bryony Thompson Gene: ikbkg has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.9 IKBKG Bryony Thompson gene: IKBKG was added
gene: IKBKG was added to Ectodermal Dysplasia_RMH. Sources: Expert list
Mode of inheritance for gene: IKBKG was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Publications for gene: IKBKG were set to 10839543; 30422821
Phenotypes for gene: IKBKG were set to Ectodermal dysplasia and immunodeficiency 1 MIM3300291; Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency MIM#300301; Incontinentia pigmenti MIM#308300
Review for gene: IKBKG was set to GREEN
Added comment: Ectodermal dysplasia is a feature of the condition. >3 cases reported.
Sources: Expert list
Mitochondrial disease v0.128 HLCS Zornitza Stark Marked gene: HLCS as ready
Mitochondrial disease v0.128 HLCS Zornitza Stark Gene: hlcs has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.128 HLCS Zornitza Stark Classified gene: HLCS as Amber List (moderate evidence)
Mitochondrial disease v0.128 HLCS Zornitza Stark Gene: hlcs has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.127 HLCS Zornitza Stark gene: HLCS was added
gene: HLCS was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: HLCS was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: HLCS were set to Holocarboxylase synthetase deficiency, MIM# 253270
Review for gene: HLCS was set to AMBER
Added comment: HCS localises to nucleus. Clinical presentation is with metabolic acidosis, which could potentially mimic a mitochondrial disorder.
Sources: Expert list
Mitochondrial disease v0.126 GDAP1 Zornitza Stark Marked gene: GDAP1 as ready
Mitochondrial disease v0.126 GDAP1 Zornitza Stark Gene: gdap1 has been classified as Green List (High Evidence).
Mitochondrial disease v0.126 GDAP1 Zornitza Stark Classified gene: GDAP1 as Green List (high evidence)
Mitochondrial disease v0.126 GDAP1 Zornitza Stark Gene: gdap1 has been classified as Green List (High Evidence).
Mitochondrial disease v0.125 GDAP1 Zornitza Stark gene: GDAP1 was added
gene: GDAP1 was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: GDAP1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: GDAP1 were set to 16172208; 21753178; 21365284; 20232219; 11743580
Phenotypes for gene: GDAP1 were set to Charcot-Marie-Tooth disease, axonal, type 2K 607831, MIM# Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, MIM# 607706; Charcot-Marie-Tooth disease, recessive intermediate, A, MIM# 608340; Charcot-Marie-Tooth disease, type 4A, MIM# 214400
Review for gene: GDAP1 was set to GREEN
Added comment: GDAP1 is an integral membrane protein of the outer mitochondrial membrane. Overexpression of Gdap1 induces fragmentation of mitochondria without inducing apoptosis, affecting overall mitochondrial activity, or interfering with mitochondrial fusion. Gdap1-specific knockdown by RNA interference resulted in a tubular mitochondrial morphology.
Sources: Expert list
Ectodermal Dysplasia v0.8 IFT43 Bryony Thompson changed review comment from: Two unrelated families with cranioectodermal dysplasia and the same variant, p.M1V. The gene is also associated with short-rib thoracic dysplasia, which is also a gene list.
Sources: Expert list; to: Two unrelated families with cranioectodermal dysplasia and the same variant, p.M1V. The gene is also associated with short-rib thoracic dysplasia, a skeletal ciliopathy.
Sources: Expert list
Mitochondrial disease v0.124 FXN Zornitza Stark Marked gene: FXN as ready
Mitochondrial disease v0.124 FXN Zornitza Stark Gene: fxn has been classified as Green List (High Evidence).
Mitochondrial disease v0.124 FXN Zornitza Stark Phenotypes for gene: FXN were changed from to Friedreich ataxia, MIM# 229300
Mitochondrial disease v0.123 FXN Zornitza Stark Publications for gene: FXN were set to
Mitochondrial disease v0.122 FXN Zornitza Stark Mode of inheritance for gene: FXN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.121 FXN Zornitza Stark reviewed gene: FXN: Rating: GREEN; Mode of pathogenicity: None; Publications: 10500103, 11351132; Phenotypes: Friedreich ataxia, MIM# 229300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.121 ETFB Zornitza Stark Marked gene: ETFB as ready
Mitochondrial disease v0.121 ETFB Zornitza Stark Gene: etfb has been classified as Green List (High Evidence).
Mitochondrial disease v0.121 ETFA Zornitza Stark Marked gene: ETFA as ready
Mitochondrial disease v0.121 ETFA Zornitza Stark Gene: etfa has been classified as Green List (High Evidence).
Mendeliome v0.1695 ERCC6L2 Zornitza Stark Marked gene: ERCC6L2 as ready
Mendeliome v0.1695 ERCC6L2 Zornitza Stark Gene: ercc6l2 has been classified as Green List (High Evidence).
Mendeliome v0.1695 ERCC6L2 Zornitza Stark Phenotypes for gene: ERCC6L2 were changed from to Bone marrow failure syndrome 2, MIM# 615715
Mendeliome v0.1694 ERCC6L2 Zornitza Stark Publications for gene: ERCC6L2 were set to
Mendeliome v0.1693 ERCC6L2 Zornitza Stark Mode of inheritance for gene: ERCC6L2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1692 ERCC6L2 Zornitza Stark reviewed gene: ERCC6L2: Rating: GREEN; Mode of pathogenicity: None; Publications: 24507776, 27185855; Phenotypes: Bone marrow failure syndrome 2, MIM# 615715; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.121 ERCC6L2 Zornitza Stark Marked gene: ERCC6L2 as ready
Mitochondrial disease v0.121 ERCC6L2 Zornitza Stark Added comment: Comment when marking as ready: Agree, not in the scope of this panel.
Mitochondrial disease v0.121 ERCC6L2 Zornitza Stark Gene: ercc6l2 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.121 ERCC6L2 Zornitza Stark Phenotypes for gene: ERCC6L2 were changed from to Bone marrow failure syndrome 2, MIM#615715
Mitochondrial disease v0.120 ERCC6L2 Zornitza Stark Publications for gene: ERCC6L2 were set to
Mitochondrial disease v0.120 ERCC6L2 Zornitza Stark Mode of inheritance for gene: ERCC6L2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.119 ERCC6L2 Zornitza Stark Classified gene: ERCC6L2 as Red List (low evidence)
Mitochondrial disease v0.119 ERCC6L2 Zornitza Stark Gene: ercc6l2 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2464 GPT2 Chern Lim reviewed gene: GPT2: Rating: GREEN; Mode of pathogenicity: None; Publications: 27601654, 25758935; Phenotypes: Mental retardation, autosomal recessive 49, MIM#616281; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.118 DNM2 Zornitza Stark Marked gene: DNM2 as ready
Mitochondrial disease v0.118 DNM2 Zornitza Stark Gene: dnm2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.118 DNM2 Zornitza Stark Classified gene: DNM2 as Green List (high evidence)
Mitochondrial disease v0.118 DNM2 Zornitza Stark Gene: dnm2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.117 DNM2 Zornitza Stark gene: DNM2 was added
gene: DNM2 was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: DNM2 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes for gene: DNM2 were set to Centronuclear myopathy 1 160150 AD 3 Charcot-Marie-Tooth disease, axonal type 2M, MIM# 606482; Charcot-Marie-Tooth disease, dominant intermediate B, MIM# 606482; Lethal congenital contracture syndrome 5, MIM# 615368
Review for gene: DNM2 was set to GREEN
gene: DNM2 was marked as current diagnostic
Added comment: Involved in mitochondrial division, histopathological abnormalities affecting mitochondria reported. Neuromuscular presentation, AR variants are thought to be hypomorphic.
Sources: Expert list
Mitochondrial disease v0.116 CYCS Zornitza Stark Marked gene: CYCS as ready
Mitochondrial disease v0.116 CYCS Zornitza Stark Gene: cycs has been classified as Green List (High Evidence).
Mitochondrial disease v0.116 CYCS Zornitza Stark Phenotypes for gene: CYCS were changed from to Thrombocytopenia 4, MIM#612004
Mitochondrial disease v0.115 CYCS Zornitza Stark Publications for gene: CYCS were set to
Mitochondrial disease v0.114 CYCS Zornitza Stark Mode of inheritance for gene: CYCS was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mitochondrial disease v0.113 CA5A Zornitza Stark Marked gene: CA5A as ready
Mitochondrial disease v0.113 CA5A Zornitza Stark Gene: ca5a has been classified as Green List (High Evidence).
Mitochondrial disease v0.113 CA5A Zornitza Stark Classified gene: CA5A as Green List (high evidence)
Mitochondrial disease v0.113 CA5A Zornitza Stark Gene: ca5a has been classified as Green List (High Evidence).
Mitochondrial disease v0.112 CA5A Zornitza Stark gene: CA5A was added
gene: CA5A was added to Mitochondrial disease. Sources: Expert list
Mode of inheritance for gene: CA5A was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: CA5A were set to Hyperammonemia due to carbonic anhydrase VA deficiency, MIM# 615751
Review for gene: CA5A was set to GREEN
Added comment: Acute onset of encephalopathy in infancy or early childhood with metabolic acidosis and respiratory alkalosis, hypoglycemia, increased serum lactate and alanine, and evidence of impaired provision of bicarbonate to essential mitochondrial enzymes. Episodic acute events in early childhood with intercurrent illness but relatively limited neurological sequelae.
Sources: Expert list
Mendeliome v0.1692 PPM1E Zornitza Stark Marked gene: PPM1E as ready
Mendeliome v0.1692 PPM1E Zornitza Stark Added comment: Comment when marking as ready: Agreed, cannot find evidence for Mendelian gene-disease association.
Mendeliome v0.1692 PPM1E Zornitza Stark Gene: ppm1e has been classified as Red List (Low Evidence).
Mendeliome v0.1692 PPM1E Zornitza Stark Classified gene: PPM1E as Red List (low evidence)
Mendeliome v0.1692 PPM1E Zornitza Stark Gene: ppm1e has been classified as Red List (Low Evidence).
Mendeliome v0.1691 PPM1E Naomi Baker reviewed gene: PPM1E: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Usher Syndrome v0.4 USH1C Zornitza Stark Marked gene: USH1C as ready
Usher Syndrome v0.4 USH1C Zornitza Stark Gene: ush1c has been classified as Green List (High Evidence).
Usher Syndrome v0.4 USH1C Teresa Zhao reviewed gene: USH1C: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Deafness, autosomal recessive 18A, 602092, Usher syndrome, type 1C, 276904; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2463 SUPT16H Zornitza Stark Marked gene: SUPT16H as ready
Intellectual disability syndromic and non-syndromic v0.2463 SUPT16H Zornitza Stark Gene: supt16h has been classified as Green List (High Evidence).
Dilated Cardiomyopathy v0.20 LAMP2 Zornitza Stark Marked gene: LAMP2 as ready
Dilated Cardiomyopathy v0.20 LAMP2 Zornitza Stark Gene: lamp2 has been classified as Green List (High Evidence).
Dilated Cardiomyopathy v0.20 LAMP2 Zornitza Stark Phenotypes for gene: LAMP2 were changed from to Danon disease, MIM#300257
Dilated Cardiomyopathy v0.19 LAMP2 Zornitza Stark Publications for gene: LAMP2 were set to
Dilated Cardiomyopathy v0.18 LAMP2 Zornitza Stark Mode of inheritance for gene: LAMP2 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Callosome v0.109 SUPT16H Zornitza Stark Marked gene: SUPT16H as ready
Callosome v0.109 SUPT16H Zornitza Stark Gene: supt16h has been classified as Green List (High Evidence).
Callosome v0.109 SUPT16H Zornitza Stark Classified gene: SUPT16H as Green List (high evidence)
Callosome v0.109 SUPT16H Zornitza Stark Gene: supt16h has been classified as Green List (High Evidence).
Callosome v0.108 SUPT16H Zornitza Stark gene: SUPT16H was added
gene: SUPT16H was added to Callosome. Sources: Literature
Mode of inheritance for gene: SUPT16H was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SUPT16H were set to 31924697
Phenotypes for gene: SUPT16H were set to Intellectual disability; Abnormality of the corpus callosum
Review for gene: SUPT16H was set to GREEN
Added comment: Four unrelated individuals with de novo missense variants in this gene. Publication also reports on a deletion, but note this includes other genes and the individual also had another CNV.
Sources: Literature
Mendeliome v0.1691 SUPT16H Zornitza Stark Marked gene: SUPT16H as ready
Mendeliome v0.1691 SUPT16H Zornitza Stark Gene: supt16h has been classified as Green List (High Evidence).
Mendeliome v0.1691 SUPT16H Zornitza Stark Classified gene: SUPT16H as Green List (high evidence)
Mendeliome v0.1691 SUPT16H Zornitza Stark Gene: supt16h has been classified as Green List (High Evidence).
Mendeliome v0.1690 SUPT16H Zornitza Stark gene: SUPT16H was added
gene: SUPT16H was added to Mendeliome. Sources: Literature
Mode of inheritance for gene: SUPT16H was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SUPT16H were set to 31924697
Phenotypes for gene: SUPT16H were set to Intellectual disability; Abnormality of the corpus callosum
Review for gene: SUPT16H was set to GREEN
Added comment: Four unrelated individuals with de novo missense variants in this gene. Publication also reports on a deletion, but note this includes other genes and the individual also had another CNV.
Sources: Literature
Intellectual disability syndromic and non-syndromic v0.2463 SUPT16H Zornitza Stark Classified gene: SUPT16H as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2463 SUPT16H Zornitza Stark Gene: supt16h has been classified as Green List (High Evidence).
Dilated Cardiomyopathy v0.17 LAMP2 Teresa Zhao reviewed gene: LAMP2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 25228319, 27165304; Phenotypes: Danon disease, 300257; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Intellectual disability syndromic and non-syndromic v0.2462 SUPT16H Zornitza Stark gene: SUPT16H was added
gene: SUPT16H was added to Intellectual disability syndromic and non-syndromic. Sources: Literature
Mode of inheritance for gene: SUPT16H was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SUPT16H were set to 31924697
Phenotypes for gene: SUPT16H were set to Intellectual disability; Abnormality of the corpus callosum
Review for gene: SUPT16H was set to GREEN
Added comment: Four unrelated individuals with de novo missense variants in this gene. Publication also reports on a deletion, but note this includes other genes and the individual also had another CNV.
Sources: Literature
Intellectual disability syndromic and non-syndromic v0.2461 SLC5A6 Zornitza Stark Publications for gene: SLC5A6 were set to 31754459; 27904971
Intellectual disability syndromic and non-syndromic v0.2460 SLC5A6 Zornitza Stark changed review comment from: Two unrelated families reported, functional data and some evidence of response to treatment.
Sources: Literature; to: Three unrelated families reported, functional data and some evidence of response to treatment.
Sources: Literature
Intellectual disability syndromic and non-syndromic v0.2460 SLC5A6 Zornitza Stark edited their review of gene: SLC5A6: Changed publications: 31754459, 27904971, 31392107
Mendeliome v0.1689 RARS Zornitza Stark Marked gene: RARS as ready
Mendeliome v0.1689 RARS Zornitza Stark Gene: rars has been classified as Green List (High Evidence).
Mendeliome v0.1689 RARS Zornitza Stark Phenotypes for gene: RARS were changed from to Leukodystrophy, hypomyelinating, 9 MIM# 616140
Mendeliome v0.1688 RARS Zornitza Stark Publications for gene: RARS were set to
Mendeliome v0.1687 RARS Zornitza Stark Mode of inheritance for gene: RARS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1686 RARS Zornitza Stark reviewed gene: RARS: Rating: GREEN; Mode of pathogenicity: None; Publications: 31814314; Phenotypes: Leukodystrophy, hypomyelinating, 9 MIM# 616140; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2460 RARS Zornitza Stark Marked gene: RARS as ready
Intellectual disability syndromic and non-syndromic v0.2460 RARS Zornitza Stark Gene: rars has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2460 RARS Zornitza Stark Classified gene: RARS as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2460 RARS Zornitza Stark Gene: rars has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2459 RARS Zornitza Stark gene: RARS was added
gene: RARS was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: RARS was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: RARS were set to 31814314
Phenotypes for gene: RARS were set to Leukodystrophy, hypomyelinating, 9 MIM# 616140
Review for gene: RARS was set to GREEN
gene: RARS was marked as current diagnostic
Added comment: 15 families reported, DD/ID is part of the phenotype.
Sources: Expert list
Mendeliome v0.1686 CXorf56 Zornitza Stark Classified gene: CXorf56 as Green List (high evidence)
Mendeliome v0.1686 CXorf56 Zornitza Stark Gene: cxorf56 has been classified as Green List (High Evidence).
Mendeliome v0.1685 CXorf56 Zornitza Stark edited their review of gene: CXorf56: Added comment: Additional 3 families reported, upgrade to Green.; Changed rating: GREEN; Changed publications: 29374277, 31822863; Changed phenotypes: Mental retardation, X-linked 107, MIM# 301013
Intellectual disability syndromic and non-syndromic v0.2458 CXorf56 Zornitza Stark Classified gene: CXorf56 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2458 CXorf56 Zornitza Stark Gene: cxorf56 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2457 CXorf56 Zornitza Stark edited their review of gene: CXorf56: Added comment: Additional report of three more families, upgrade to Green.; Changed rating: GREEN; Changed publications: 29374277, 31822863; Changed phenotypes: Mental retardation, X-linked 107, MIM# 301013
Ectodermal Dysplasia v0.8 IFT43 Bryony Thompson Marked gene: IFT43 as ready
Ectodermal Dysplasia v0.8 IFT43 Bryony Thompson Gene: ift43 has been classified as Amber List (Moderate Evidence).
Ectodermal Dysplasia v0.8 IFT43 Bryony Thompson Classified gene: IFT43 as Amber List (moderate evidence)
Ectodermal Dysplasia v0.8 IFT43 Bryony Thompson Gene: ift43 has been classified as Amber List (Moderate Evidence).
Ectodermal Dysplasia v0.7 IFT43 Bryony Thompson gene: IFT43 was added
gene: IFT43 was added to Ectodermal Dysplasia_RMH. Sources: Expert list
Mode of inheritance for gene: IFT43 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: IFT43 were set to 21378380; 29896747
Phenotypes for gene: IFT43 were set to Cranioectodermal dysplasia 3 MIM#614099
Review for gene: IFT43 was set to AMBER
Added comment: Two unrelated families with cranioectodermal dysplasia and the same variant, p.M1V. The gene is also associated with short-rib thoracic dysplasia, which is also a gene list.
Sources: Expert list
Mendeliome v0.1685 TNR Zornitza Stark Marked gene: TNR as ready
Mendeliome v0.1685 TNR Zornitza Stark Gene: tnr has been classified as Green List (High Evidence).
Mendeliome v0.1685 TNR Zornitza Stark Classified gene: TNR as Green List (high evidence)
Mendeliome v0.1685 TNR Zornitza Stark Gene: tnr has been classified as Green List (High Evidence).
Mendeliome v0.1684 TNR Zornitza Stark gene: TNR was added
gene: TNR was added to Mendeliome. Sources: Literature
Mode of inheritance for gene: TNR was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TNR were set to 32099069
Phenotypes for gene: TNR were set to Spastic para- or tetraparesis; Axial muscular hypotonia; Intellectual disability; Transient opisthotonus
Review for gene: TNR was set to GREEN
Added comment: 13 individuals from 8 unrelated families reported.
Sources: Literature
Cerebral Palsy v0.14 TNR Zornitza Stark Marked gene: TNR as ready
Cerebral Palsy v0.14 TNR Zornitza Stark Gene: tnr has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.6 CTNND1 Bryony Thompson Marked gene: CTNND1 as ready
Ectodermal Dysplasia v0.6 CTNND1 Bryony Thompson Gene: ctnnd1 has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.6 CTNND1 Bryony Thompson Classified gene: CTNND1 as Green List (high evidence)
Ectodermal Dysplasia v0.6 CTNND1 Bryony Thompson Gene: ctnnd1 has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.5 CTNND1 Bryony Thompson gene: CTNND1 was added
gene: CTNND1 was added to Ectodermal Dysplasia_RMH. Sources: Expert list
Mode of inheritance for gene: CTNND1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CTNND1 were set to 28301459
Phenotypes for gene: CTNND1 were set to Blepharocheilodontic syndrome 2 MIM#617681
Review for gene: CTNND1 was set to GREEN
Added comment: Ectodermal dysplasia is a feature of the condition. Four cases from three unrelated families.
Sources: Expert list
Cerebral Palsy v0.14 TNR Zornitza Stark Classified gene: TNR as Green List (high evidence)
Cerebral Palsy v0.14 TNR Zornitza Stark Gene: tnr has been classified as Green List (High Evidence).
Cerebral Palsy v0.13 TNR Zornitza Stark gene: TNR was added
gene: TNR was added to Cerebral Palsy. Sources: Expert list
Mode of inheritance for gene: TNR was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TNR were set to 32099069
Phenotypes for gene: TNR were set to Spastic para- or tetraparesis; Axial muscular hypotonia; Intellectual disability; Transient opisthotonus
Review for gene: TNR was set to GREEN
Added comment: 13 individuals from 8 unrelated families reported.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2457 TNR Zornitza Stark Marked gene: TNR as ready
Intellectual disability syndromic and non-syndromic v0.2457 TNR Zornitza Stark Gene: tnr has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.4 CHD1 Bryony Thompson Marked gene: CHD1 as ready
Ectodermal Dysplasia v0.4 CHD1 Bryony Thompson Gene: chd1 has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.4 CHD1 Bryony Thompson Classified gene: CHD1 as Green List (high evidence)
Ectodermal Dysplasia v0.4 CHD1 Bryony Thompson Gene: chd1 has been classified as Green List (High Evidence).
Ectodermal Dysplasia v0.3 CHD1 Bryony Thompson gene: CHD1 was added
gene: CHD1 was added to Ectodermal Dysplasia_RMH. Sources: Expert list
Mode of inheritance for gene: CHD1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CHD1 were set to 28866611
Phenotypes for gene: CHD1 were set to Pilarowski-Bjornsson syndrome MIM#617682
Review for gene: CHD1 was set to GREEN
Added comment: Phenotype includes at least two ectodermal structures: translucent skin and cranial-facial feature. >3 cases with mostly de novo variants.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2457 TNR Zornitza Stark Classified gene: TNR as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2457 TNR Zornitza Stark Gene: tnr has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2456 TNR Zornitza Stark gene: TNR was added
gene: TNR was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: TNR was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TNR were set to 32099069
Phenotypes for gene: TNR were set to Spastic para- or tetraparesis; Axial muscular hypotonia; Intellectual disability; Transient opisthotonus
Review for gene: TNR was set to GREEN
Added comment: 13 individuals from 8 unrelated families reported.
Sources: Expert list
Skeletal dysplasia v0.10 RSPRY1 Zornitza Stark Marked gene: RSPRY1 as ready
Skeletal dysplasia v0.10 RSPRY1 Zornitza Stark Gene: rspry1 has been classified as Amber List (Moderate Evidence).
Skeletal dysplasia v0.10 RSPRY1 Zornitza Stark Classified gene: RSPRY1 as Amber List (moderate evidence)
Skeletal dysplasia v0.10 RSPRY1 Zornitza Stark Gene: rspry1 has been classified as Amber List (Moderate Evidence).
Skeletal dysplasia v0.9 RSPRY1 Zornitza Stark gene: RSPRY1 was added
gene: RSPRY1 was added to Skeletal dysplasia. Sources: Expert list
Mode of inheritance for gene: RSPRY1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: RSPRY1 were set to 26365341
Phenotypes for gene: RSPRY1 were set to Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type, 616585
Review for gene: RSPRY1 was set to AMBER
Added comment: Two unrelated individuals reported, some functional evidence.
Sources: Expert list
Mendeliome v0.1683 RSPRY1 Zornitza Stark Marked gene: RSPRY1 as ready
Mendeliome v0.1683 RSPRY1 Zornitza Stark Gene: rspry1 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1683 RSPRY1 Zornitza Stark Phenotypes for gene: RSPRY1 were changed from to Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type, 616585
Mendeliome v0.1682 RSPRY1 Zornitza Stark Publications for gene: RSPRY1 were set to
Mendeliome v0.1681 RSPRY1 Zornitza Stark Mode of inheritance for gene: RSPRY1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1680 RSPRY1 Zornitza Stark Classified gene: RSPRY1 as Amber List (moderate evidence)
Mendeliome v0.1680 RSPRY1 Zornitza Stark Gene: rspry1 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2455 RSPRY1 Zornitza Stark changed review comment from: Two unrelated individuals reported, some functional evidence.
Sources: Expert list; to: Two unrelated individuals reported, some functional evidence. Dev delay/autism part of the phenotype.
Sources: Expert list
Mendeliome v0.1679 RSPRY1 Zornitza Stark reviewed gene: RSPRY1: Rating: AMBER; Mode of pathogenicity: None; Publications: 26365341; Phenotypes: Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type, 616585; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2455 RSPRY1 Zornitza Stark Classified gene: RSPRY1 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2455 RSPRY1 Zornitza Stark Gene: rspry1 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2454 RSPRY1 Zornitza Stark gene: RSPRY1 was added
gene: RSPRY1 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: RSPRY1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: RSPRY1 were set to 26365341
Phenotypes for gene: RSPRY1 were set to Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type, 616585
Review for gene: RSPRY1 was set to AMBER
Added comment: Two unrelated individuals reported, some functional evidence.
Sources: Expert list
Hypertrichosis syndromes v0.13 RPS23 Zornitza Stark Marked gene: RPS23 as ready
Hypertrichosis syndromes v0.13 RPS23 Zornitza Stark Gene: rps23 has been classified as Amber List (Moderate Evidence).
Hypertrichosis syndromes v0.13 RPS23 Zornitza Stark Phenotypes for gene: RPS23 were changed from to Brachycephaly, trichomegaly, and developmental delay, MIM# 617412
Hypertrichosis syndromes v0.12 RPS23 Zornitza Stark Publications for gene: RPS23 were set to
Hypertrichosis syndromes v0.11 RPS23 Zornitza Stark Mode of inheritance for gene: RPS23 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hypertrichosis syndromes v0.10 RPS23 Zornitza Stark Classified gene: RPS23 as Amber List (moderate evidence)
Hypertrichosis syndromes v0.10 RPS23 Zornitza Stark Gene: rps23 has been classified as Amber List (Moderate Evidence).
Hypertrichosis syndromes v0.9 RPS23 Zornitza Stark reviewed gene: RPS23: Rating: AMBER; Mode of pathogenicity: None; Publications: 28257692; Phenotypes: Brachycephaly, trichomegaly, and developmental delay, MIM# 617412; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2453 RPS23 Zornitza Stark Phenotypes for gene: RPS23 were changed from Brachycephaly, trichomegaly, and developmental delay, MIM# 617412 to Brachycephaly, trichomegaly, and developmental delay, MIM# 617412
Mendeliome v0.1679 RPS23 Zornitza Stark Marked gene: RPS23 as ready
Mendeliome v0.1679 RPS23 Zornitza Stark Gene: rps23 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2453 RPS23 Zornitza Stark Marked gene: RPS23 as ready
Intellectual disability syndromic and non-syndromic v0.2453 RPS23 Zornitza Stark Gene: rps23 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1679 RPS23 Zornitza Stark Phenotypes for gene: RPS23 were changed from to Brachycephaly, trichomegaly, and developmental delay, MIM# 617412
Intellectual disability syndromic and non-syndromic v0.2453 RPS23 Zornitza Stark Phenotypes for gene: RPS23 were changed from to Brachycephaly, trichomegaly, and developmental delay, MIM# 617412
Intellectual disability syndromic and non-syndromic v0.2452 RPS23 Zornitza Stark Publications for gene: RPS23 were set to 28257692
Intellectual disability syndromic and non-syndromic v0.2452 RPS23 Zornitza Stark Publications for gene: RPS23 were set to
Mendeliome v0.1678 RPS23 Zornitza Stark Publications for gene: RPS23 were set to
Mendeliome v0.1677 RPS23 Zornitza Stark Mode of inheritance for gene: RPS23 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1676 RPS23 Zornitza Stark Mode of inheritance for gene: RPS23 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1675 RPS23 Zornitza Stark Classified gene: RPS23 as Amber List (moderate evidence)
Mendeliome v0.1675 RPS23 Zornitza Stark Gene: rps23 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1674 RPS23 Zornitza Stark reviewed gene: RPS23: Rating: AMBER; Mode of pathogenicity: None; Publications: 28257692; Phenotypes: Brachycephaly, trichomegaly, and developmental delay, MIM# 617412; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2451 RPS23 Zornitza Stark Mode of inheritance for gene: RPS23 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2450 RPS23 Zornitza Stark Classified gene: RPS23 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2450 RPS23 Zornitza Stark Gene: rps23 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2449 RPS23 Zornitza Stark reviewed gene: RPS23: Rating: AMBER; Mode of pathogenicity: None; Publications: 28257692; Phenotypes: Brachycephaly, trichomegaly, and developmental delay, MIM# 617412; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2449 RNF13 Zornitza Stark Marked gene: RNF13 as ready
Intellectual disability syndromic and non-syndromic v0.2449 RNF13 Zornitza Stark Gene: rnf13 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2449 RNF13 Zornitza Stark Classified gene: RNF13 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2449 RNF13 Zornitza Stark Gene: rnf13 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2448 RNF13 Zornitza Stark gene: RNF13 was added
gene: RNF13 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: RNF13 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: RNF13 were set to 30595371
Phenotypes for gene: RNF13 were set to Epileptic encephalopathy, early infantile, 73 618379
Mode of pathogenicity for gene: RNF13 was set to Other
Review for gene: RNF13 was set to GREEN
Added comment: Three unrelated individuals with de novo variants in this gene and severe neurological phenotype, including microcephaly, seizures, visual impairment, profound developmental delay.
Sources: Expert list
Autism v0.77 RIMS1 Zornitza Stark Phenotypes for gene: RIMS1 were changed from to Autism
Autism v0.76 RIMS1 Zornitza Stark Publications for gene: RIMS1 were set to
Autism v0.75 RIMS1 Zornitza Stark Mode of inheritance for gene: RIMS1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Autism v0.74 RIMS1 Zornitza Stark reviewed gene: RIMS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25284784, 25961944; Phenotypes: Autism; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2447 RIMS1 Zornitza Stark Marked gene: RIMS1 as ready
Intellectual disability syndromic and non-syndromic v0.2447 RIMS1 Zornitza Stark Gene: rims1 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2447 RIMS1 Zornitza Stark Phenotypes for gene: RIMS1 were changed from to Autism; Cone-rod dystrophy 7 , MIM#603649
Intellectual disability syndromic and non-syndromic v0.2446 RIMS1 Zornitza Stark Publications for gene: RIMS1 were set to
Intellectual disability syndromic and non-syndromic v0.2445 RIMS1 Zornitza Stark Mode of inheritance for gene: RIMS1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2444 RIMS1 Zornitza Stark Classified gene: RIMS1 as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2444 RIMS1 Zornitza Stark Gene: rims1 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2443 RIMS1 Zornitza Stark reviewed gene: RIMS1: Rating: RED; Mode of pathogenicity: None; Publications: 25284784, 12659814; Phenotypes: Autism, Cone-rod dystrophy 7 , MIM#603649; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2443 RHEB Zornitza Stark Marked gene: RHEB as ready
Intellectual disability syndromic and non-syndromic v0.2443 RHEB Zornitza Stark Gene: rheb has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2443 RHEB Zornitza Stark Phenotypes for gene: RHEB were changed from to Intellectual disability; Macrocephaly; Focal cortical dysplasia
Intellectual disability syndromic and non-syndromic v0.2442 RHEB Zornitza Stark Publications for gene: RHEB were set to
Intellectual disability syndromic and non-syndromic v0.2441 RHEB Zornitza Stark Mode of inheritance for gene: RHEB was changed from Unknown to Other
Intellectual disability syndromic and non-syndromic v0.2440 RHEB Zornitza Stark reviewed gene: RHEB: Rating: GREEN; Mode of pathogenicity: None; Publications: 31337748, 29051493; Phenotypes: Intellectual disability, Macrocephaly, Focal cortical dysplasia; Mode of inheritance: Other
Mitochondrial disease v0.111 MRPS34 Zornitza Stark Phenotypes for gene: MRPS34 were changed from to Combined oxidative phosphorylation deficiency 32, MIM# 617664
Mitochondrial disease v0.110 MRPS34 Zornitza Stark Publications for gene: MRPS34 were set to
Mitochondrial disease v0.109 MRPS34 Zornitza Stark Mode of inheritance for gene: MRPS34 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.108 MRPS34 Zornitza Stark reviewed gene: MRPS34: Rating: GREEN; Mode of pathogenicity: None; Publications: 28777931; Phenotypes: Combined oxidative phosphorylation deficiency 32, MIM# 617664; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2440 MRPS34 Zornitza Stark Marked gene: MRPS34 as ready
Intellectual disability syndromic and non-syndromic v0.2440 MRPS34 Zornitza Stark Gene: mrps34 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2440 MRPS34 Zornitza Stark Classified gene: MRPS34 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2440 MRPS34 Zornitza Stark Gene: mrps34 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2439 MRPS34 Zornitza Stark gene: MRPS34 was added
gene: MRPS34 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: MRPS34 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MRPS34 were set to 28777931
Phenotypes for gene: MRPS34 were set to Combined oxidative phosphorylation deficiency 32, MIM# 617664
Review for gene: MRPS34 was set to GREEN
gene: MRPS34 was marked as current diagnostic
Added comment: Six individuals from 4 unrelated families; clinical presentation is with developmental delay/regression. More variable features include movement disorders, microcephaly, strabismus, nystagmus, optic atrophy.
Sources: Expert list
Mendeliome v0.1674 KANK1 Zornitza Stark Classified gene: KANK1 as Red List (low evidence)
Mendeliome v0.1674 KANK1 Zornitza Stark Gene: kank1 has been classified as Red List (Low Evidence).
Mendeliome v0.1673 KANK1 Zornitza Stark changed review comment from: Comment on list classification: Amber for nephrotic after discussion with Chirag Patel.; to: Comment on list classification: Red for nephrotic after discussion with Chirag Patel.
Mendeliome v0.1673 FUT6 Zornitza Stark Marked gene: FUT6 as ready
Mendeliome v0.1673 FUT6 Zornitza Stark Gene: fut6 has been classified as Red List (Low Evidence).
Mendeliome v0.1673 FUT6 Zornitza Stark Phenotypes for gene: FUT6 were changed from to Fucosyltransferase 6 deficiency, MIM# 613852
Mendeliome v0.1672 FUT6 Zornitza Stark Classified gene: FUT6 as Red List (low evidence)
Mendeliome v0.1672 FUT6 Zornitza Stark Gene: fut6 has been classified as Red List (Low Evidence).
Mendeliome v0.1671 FUT6 Zornitza Stark reviewed gene: FUT6: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Fucosyltransferase 6 deficiency, MIM# 613852; Mode of inheritance: None
Mendeliome v0.1671 FUT2 Zornitza Stark Marked gene: FUT2 as ready
Mendeliome v0.1671 FUT2 Zornitza Stark Gene: fut2 has been classified as Red List (Low Evidence).
Mendeliome v0.1671 FUT2 Zornitza Stark Phenotypes for gene: FUT2 were changed from to [Bombay phenotype, digenic] 616754; {Norwalk virus infection, resistance to}; {Vitamin B12 plasma level QTL1} 612542
Mendeliome v0.1670 FUT2 Zornitza Stark Classified gene: FUT2 as Red List (low evidence)
Mendeliome v0.1670 FUT2 Zornitza Stark Gene: fut2 has been classified as Red List (Low Evidence).
Mendeliome v0.1669 FUT2 Zornitza Stark reviewed gene: FUT2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: [Bombay phenotype, digenic] 616754, {Norwalk virus infection, resistance to}, {Vitamin B12 plasma level QTL1} 612542; Mode of inheritance: None
Congenital Disorders of Glycosylation v0.42 SSR4 Zornitza Stark Marked gene: SSR4 as ready
Congenital Disorders of Glycosylation v0.42 SSR4 Zornitza Stark Gene: ssr4 has been classified as Green List (High Evidence).
Congenital Disorders of Glycosylation v0.42 SSR4 Zornitza Stark Classified gene: SSR4 as Green List (high evidence)
Congenital Disorders of Glycosylation v0.42 SSR4 Zornitza Stark Gene: ssr4 has been classified as Green List (High Evidence).
Congenital Disorders of Glycosylation v0.41 SSR4 Zornitza Stark gene: SSR4 was added
gene: SSR4 was added to Congenital Disorders of Glycosylation. Sources: Expert list
Mode of inheritance for gene: SSR4 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes for gene: SSR4 were set to Congenital disorder of glycosylation, type Iy, MIM#300934
Review for gene: SSR4 was set to GREEN
Added comment: Sources: Expert list
Mendeliome v0.1669 HMGA2 Zornitza Stark Marked gene: HMGA2 as ready
Mendeliome v0.1669 HMGA2 Zornitza Stark Gene: hmga2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1669 HMGA2 Zornitza Stark Phenotypes for gene: HMGA2 were changed from to Silver-Russel syndrome
Mendeliome v0.1668 HMGA2 Zornitza Stark Publications for gene: HMGA2 were set to
Mendeliome v0.1667 HMGA2 Zornitza Stark Mode of inheritance for gene: HMGA2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1666 HMGA2 Zornitza Stark Tag SV/CNV tag was added to gene: HMGA2.
Mendeliome v0.1666 HMGA2 Zornitza Stark Classified gene: HMGA2 as Amber List (moderate evidence)
Mendeliome v0.1666 HMGA2 Zornitza Stark Gene: hmga2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1665 HMGA2 Zornitza Stark reviewed gene: HMGA2: Rating: AMBER; Mode of pathogenicity: None; Publications: 29655892, 25809938; Phenotypes: Silver-Russel syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1665 DTD1 Zornitza Stark Marked gene: DTD1 as ready
Mendeliome v0.1665 DTD1 Zornitza Stark Gene: dtd1 has been classified as Red List (Low Evidence).
Mendeliome v0.1665 DTD1 Zornitza Stark Classified gene: DTD1 as Red List (low evidence)
Mendeliome v0.1665 DTD1 Zornitza Stark Gene: dtd1 has been classified as Red List (Low Evidence).
Mendeliome v0.1664 DTD1 Zornitza Stark reviewed gene: DTD1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Mendeliome v0.1664 UTS2B Zornitza Stark Marked gene: UTS2B as ready
Mendeliome v0.1664 UTS2B Zornitza Stark Gene: uts2b has been classified as Red List (Low Evidence).
Mendeliome v0.1664 UTS2B Zornitza Stark Classified gene: UTS2B as Red List (low evidence)
Mendeliome v0.1664 UTS2B Zornitza Stark Gene: uts2b has been classified as Red List (Low Evidence).
Mendeliome v0.1663 UTS2B Zornitza Stark reviewed gene: UTS2B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Deafness_IsolatedAndComplex v0.328 CDC14A Lilian Downie commented on gene: CDC14A
Ectodermal Dysplasia v0.2 CST6 Bryony Thompson Classified gene: CST6 as Amber List (moderate evidence)
Ectodermal Dysplasia v0.2 CST6 Bryony Thompson Gene: cst6 has been classified as Amber List (Moderate Evidence).
Ectodermal Dysplasia v0.1 CST6 Bryony Thompson reviewed gene: CST6: Rating: AMBER; Mode of pathogenicity: None; Publications: 30425301; Phenotypes: Ectodermal dysplasia 15, hypohidrotic/hair type MIM#618535; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ectodermal Dysplasia v0.1 BCS1L Bryony Thompson reviewed gene: BCS1L: Rating: GREEN; Mode of pathogenicity: None; Publications: 24172246, 17314340, 9545407; Phenotypes: Bjornstad syndrome MIM#262000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ectodermal Dysplasia v0.1 Bryony Thompson Panel types changed to Royal Melbourne Hospital; Rare Disease
Hereditary Spastic Paraplegia - adult onset v0.6 Bryony Thompson Panel name changed from Hereditary Spastic Paraplegia - adult onset_RMH to Hereditary Spastic Paraplegia - adult onset
Panel types changed to Royal Melbourne Hospital; Rare Disease
Intellectual disability syndromic and non-syndromic v0.2438 MIR17HG Zornitza Stark Tag SV/CNV tag was added to gene: MIR17HG.
Intellectual disability syndromic and non-syndromic v0.2438 MIR17HG Zornitza Stark edited their review of gene: MIR17HG: Changed rating: AMBER
Mendeliome v0.1663 MFSD2A Zornitza Stark Marked gene: MFSD2A as ready
Mendeliome v0.1663 MFSD2A Zornitza Stark Gene: mfsd2a has been classified as Green List (High Evidence).
Mendeliome v0.1663 MFSD2A Zornitza Stark Phenotypes for gene: MFSD2A were changed from to Microcephaly 15, primary, autosomal recessive, MIM# 616486
Mendeliome v0.1662 MFSD2A Zornitza Stark Publications for gene: MFSD2A were set to
Mendeliome v0.1661 MFSD2A Zornitza Stark Mode of inheritance for gene: MFSD2A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1660 MFSD2A Zornitza Stark reviewed gene: MFSD2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 26005865, 26005868, 24828044; Phenotypes: Microcephaly 15, primary, autosomal recessive, MIM# 616486; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Microcephaly v0.98 MFSD2A Zornitza Stark Marked gene: MFSD2A as ready
Microcephaly v0.98 MFSD2A Zornitza Stark Gene: mfsd2a has been classified as Green List (High Evidence).
Microcephaly v0.98 MFSD2A Zornitza Stark Phenotypes for gene: MFSD2A were changed from to Microcephaly 15, primary, autosomal recessive, MIM# 616486
Microcephaly v0.97 MFSD2A Zornitza Stark Publications for gene: MFSD2A were set to
Microcephaly v0.96 MFSD2A Zornitza Stark Mode of inheritance for gene: MFSD2A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Microcephaly v0.95 MFSD2A Zornitza Stark reviewed gene: MFSD2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 26005865, 26005868, 24828044; Phenotypes: Microcephaly 15, primary, autosomal recessive, MIM# 616486; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2438 MFSD2A Zornitza Stark Marked gene: MFSD2A as ready
Intellectual disability syndromic and non-syndromic v0.2438 MFSD2A Zornitza Stark Gene: mfsd2a has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2438 MFSD2A Zornitza Stark Classified gene: MFSD2A as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2438 MFSD2A Zornitza Stark Gene: mfsd2a has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2437 MFSD2A Zornitza Stark gene: MFSD2A was added
gene: MFSD2A was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: MFSD2A was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MFSD2A were set to 26005865; 26005868; 24828044
Phenotypes for gene: MFSD2A were set to Microcephaly 15, primary, autosomal recessive, MIM# 616486
Review for gene: MFSD2A was set to GREEN
Added comment: Three unrelated families and two animal models.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2436 MED13 Zornitza Stark Marked gene: MED13 as ready
Intellectual disability syndromic and non-syndromic v0.2436 MED13 Zornitza Stark Gene: med13 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2436 MED13 Zornitza Stark Phenotypes for gene: MED13 were changed from to Intellectual developmental disorder 61, MIM# 618009
Intellectual disability syndromic and non-syndromic v0.2435 MED13 Zornitza Stark Publications for gene: MED13 were set to
Intellectual disability syndromic and non-syndromic v0.2434 MED13 Zornitza Stark Mode of inheritance for gene: MED13 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2433 MED13 Zornitza Stark edited their review of gene: MED13: Changed rating: GREEN
Intellectual disability syndromic and non-syndromic v0.2433 MED13 Zornitza Stark reviewed gene: MED13: Rating: ; Mode of pathogenicity: None; Publications: 29740699; Phenotypes: Intellectual developmental disorder 61, MIM# 618009; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1660 MED12L Zornitza Stark Marked gene: MED12L as ready
Mendeliome v0.1660 MED12L Zornitza Stark Gene: med12l has been classified as Green List (High Evidence).
Mendeliome v0.1660 MED12L Zornitza Stark Classified gene: MED12L as Green List (high evidence)
Mendeliome v0.1660 MED12L Zornitza Stark Gene: med12l has been classified as Green List (High Evidence).
Mendeliome v0.1659 MED12L Zornitza Stark gene: MED12L was added
gene: MED12L was added to Mendeliome. Sources: Expert list
Mode of inheritance for gene: MED12L was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: MED12L were set to 31155615
Phenotypes for gene: MED12L were set to Intellectual disability; Seizures; Autism
Review for gene: MED12L was set to GREEN
Added comment: 7 individuals reported, 3 with CNVs (encompassing other genes) and 4 with SNVs (frameshift, nonsense and splice site).
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2433 MED12L Zornitza Stark Classified gene: MED12L as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2433 MED12L Zornitza Stark Gene: med12l has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2432 MED12L Zornitza Stark gene: MED12L was added
gene: MED12L was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: MED12L was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: MED12L were set to 31155615
Phenotypes for gene: MED12L were set to Intellectual disability; Seizures; Autism
Review for gene: MED12L was set to GREEN
Added comment: 7 individuals reported, 3 with CNVs (encompassing other genes) and 4 with SNVs (frameshift, nonsense and splice site).
Sources: Expert list
Mendeliome v0.1658 MCM3AP Zornitza Stark Marked gene: MCM3AP as ready
Mendeliome v0.1658 MCM3AP Zornitza Stark Gene: mcm3ap has been classified as Green List (High Evidence).
Mendeliome v0.1658 MCM3AP Zornitza Stark Classified gene: MCM3AP as Green List (high evidence)
Mendeliome v0.1658 MCM3AP Zornitza Stark Gene: mcm3ap has been classified as Green List (High Evidence).
Mendeliome v0.1657 MCM3AP Zornitza Stark gene: MCM3AP was added
gene: MCM3AP was added to Mendeliome. Sources: Expert list
Mode of inheritance for gene: MCM3AP was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MCM3AP were set to 24123876; 28633435; 28969388; 29982295
Phenotypes for gene: MCM3AP were set to Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development, MIM#618124
Review for gene: MCM3AP was set to GREEN
gene: MCM3AP was marked as current diagnostic
Added comment: At least 10 families reported.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2431 MCM3AP Zornitza Stark Marked gene: MCM3AP as ready
Intellectual disability syndromic and non-syndromic v0.2431 MCM3AP Zornitza Stark Gene: mcm3ap has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2431 MCM3AP Zornitza Stark Classified gene: MCM3AP as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2431 MCM3AP Zornitza Stark Gene: mcm3ap has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2430 MCM3AP Zornitza Stark gene: MCM3AP was added
gene: MCM3AP was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: MCM3AP was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MCM3AP were set to 24123876; 28633435; 28969388; 29982295
Phenotypes for gene: MCM3AP were set to Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development, MIM#618124
Review for gene: MCM3AP was set to GREEN
gene: MCM3AP was marked as current diagnostic
Added comment: ID is a feature in many of the reported individuals.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2429 MARS2 Zornitza Stark Classified gene: MARS2 as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2429 MARS2 Zornitza Stark Gene: mars2 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2428 MARS2 Zornitza Stark reviewed gene: MARS2: Rating: RED; Mode of pathogenicity: None; Publications: 25754315; Phenotypes: Combined oxidative phosphorylation deficiency 25, OMIM #616430; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1656 MAPRE2 Zornitza Stark Marked gene: MAPRE2 as ready
Mendeliome v0.1656 MAPRE2 Zornitza Stark Gene: mapre2 has been classified as Green List (High Evidence).
Mendeliome v0.1656 MAPRE2 Zornitza Stark Phenotypes for gene: MAPRE2 were changed from to Symmetric circumferential skin creases, congenital, 2, MIM# 616734
Mendeliome v0.1655 MAPRE2 Zornitza Stark Publications for gene: MAPRE2 were set to
Mendeliome v0.1654 MAPRE2 Zornitza Stark Mode of inheritance for gene: MAPRE2 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Mendeliome v0.1653 MAPRE2 Zornitza Stark reviewed gene: MAPRE2: Rating: GREEN; Mode of pathogenicity: None; Publications: 26637975; Phenotypes: Symmetric circumferential skin creases, congenital, 2, MIM# 616734; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2428 MAPRE2 Zornitza Stark Marked gene: MAPRE2 as ready
Intellectual disability syndromic and non-syndromic v0.2428 MAPRE2 Zornitza Stark Gene: mapre2 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2428 MAPRE2 Zornitza Stark Classified gene: MAPRE2 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2428 MAPRE2 Zornitza Stark Gene: mapre2 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2427 MAPRE2 Zornitza Stark gene: MAPRE2 was added
gene: MAPRE2 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: MAPRE2 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Publications for gene: MAPRE2 were set to 26637975
Phenotypes for gene: MAPRE2 were set to Symmetric circumferential skin creases, congenital, 2, MIM# 616734
Review for gene: MAPRE2 was set to GREEN
Added comment: ID is part of the phenotype, more severe in those with bi-allelic variants.
Sources: Expert list
Mendeliome v0.1653 PURA Zornitza Stark Marked gene: PURA as ready
Mendeliome v0.1653 PURA Zornitza Stark Gene: pura has been classified as Green List (High Evidence).
Mendeliome v0.1653 PURA Zornitza Stark Phenotypes for gene: PURA were changed from to Mental retardation, autosomal dominant 31, MIM# 616158
Mendeliome v0.1653 PURA Zornitza Stark Publications for gene: PURA were set to 25439098; 25342064; 12972605
Mendeliome v0.1652 PURA Zornitza Stark Publications for gene: PURA were set to
Mendeliome v0.1651 PURA Zornitza Stark Mode of inheritance for gene: PURA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1650 PURA Zornitza Stark reviewed gene: PURA: Rating: GREEN; Mode of pathogenicity: None; Publications: 25439098, 25342064, 12972605; Phenotypes: Mental retardation, autosomal dominant 31, MIM# 616158; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Genetic Epilepsy v0.630 PURA Zornitza Stark Marked gene: PURA as ready
Genetic Epilepsy v0.630 PURA Zornitza Stark Gene: pura has been classified as Green List (High Evidence).
Genetic Epilepsy v0.630 PURA Zornitza Stark Phenotypes for gene: PURA were changed from to Mental retardation, autosomal dominant 31, MIM# 616158
Intellectual disability syndromic and non-syndromic v0.2426 PURA Zornitza Stark Marked gene: PURA as ready
Intellectual disability syndromic and non-syndromic v0.2426 PURA Zornitza Stark Gene: pura has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2426 PURA Zornitza Stark Phenotypes for gene: PURA were changed from to Mental retardation, autosomal dominant 31, MIM# 616158
Genetic Epilepsy v0.629 PURA Zornitza Stark Publications for gene: PURA were set to
Genetic Epilepsy v0.628 PURA Zornitza Stark Mode of inheritance for gene: PURA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2425 PURA Zornitza Stark Publications for gene: PURA were set to
Genetic Epilepsy v0.627 PURA Zornitza Stark reviewed gene: PURA: Rating: GREEN; Mode of pathogenicity: None; Publications: 25439098, 25342064, 12972605; Phenotypes: Mental retardation, autosomal dominant 31, MIM# 616158; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2424 PURA Zornitza Stark Mode of inheritance for gene: PURA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2423 PURA Zornitza Stark reviewed gene: PURA: Rating: GREEN; Mode of pathogenicity: None; Publications: 25439098, 25342064, 12972605; Phenotypes: Mental retardation, autosomal dominant 31, MIM# 616158; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Microcephaly v0.95 BPTF Zornitza Stark Marked gene: BPTF as ready
Microcephaly v0.95 BPTF Zornitza Stark Gene: bptf has been classified as Green List (High Evidence).
Microcephaly v0.95 BPTF Zornitza Stark Phenotypes for gene: BPTF were changed from to Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies, MIM# 617755
Microcephaly v0.94 BPTF Zornitza Stark Publications for gene: BPTF were set to
Microcephaly v0.93 BPTF Zornitza Stark Mode of inheritance for gene: BPTF was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Microcephaly v0.92 BPTF Zornitza Stark reviewed gene: BPTF: Rating: GREEN; Mode of pathogenicity: None; Publications: 28942966; Phenotypes: Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies, MIM# 617755; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2423 BPTF Zornitza Stark Marked gene: BPTF as ready
Intellectual disability syndromic and non-syndromic v0.2423 BPTF Zornitza Stark Gene: bptf has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2423 BPTF Zornitza Stark Phenotypes for gene: BPTF were changed from to Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies AD, MIM#617755
Intellectual disability syndromic and non-syndromic v0.2422 BPTF Zornitza Stark Publications for gene: BPTF were set to
Intellectual disability syndromic and non-syndromic v0.2421 BPTF Zornitza Stark Mode of inheritance for gene: BPTF was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2420 BPTF Zornitza Stark reviewed gene: BPTF: Rating: GREEN; Mode of pathogenicity: None; Publications: 28942966; Phenotypes: Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies AD, MIM#617755; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1650 BPTF Zornitza Stark Marked gene: BPTF as ready
Mendeliome v0.1650 BPTF Zornitza Stark Gene: bptf has been classified as Green List (High Evidence).
Mendeliome v0.1650 BPTF Zornitza Stark Phenotypes for gene: BPTF were changed from to Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies AD, MIM#617755
Mendeliome v0.1649 BPTF Zornitza Stark Publications for gene: BPTF were set to
Mendeliome v0.1648 BPTF Zornitza Stark Mode of inheritance for gene: BPTF was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Callosome v0.107 TRIO Zornitza Stark Marked gene: TRIO as ready
Callosome v0.107 TRIO Zornitza Stark Gene: trio has been classified as Red List (Low Evidence).
Callosome v0.107 TRIO Zornitza Stark Phenotypes for gene: TRIO were changed from to Mental retardation, autosomal dominant 44, MIM# 617061
Callosome v0.106 TRIO Zornitza Stark Publications for gene: TRIO were set to
Callosome v0.106 TRIO Zornitza Stark Mode of inheritance for gene: TRIO was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Callosome v0.105 TRIO Zornitza Stark Classified gene: TRIO as Red List (low evidence)
Callosome v0.105 TRIO Zornitza Stark Gene: trio has been classified as Red List (Low Evidence).
Callosome v0.104 TRIO Zornitza Stark reviewed gene: TRIO: Rating: RED; Mode of pathogenicity: None; Publications: 26721934, 32109419; Phenotypes: Mental retardation, autosomal dominant 44, MIM# 617061; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1647 TRIO Zornitza Stark Marked gene: TRIO as ready
Mendeliome v0.1647 TRIO Zornitza Stark Gene: trio has been classified as Green List (High Evidence).
Mendeliome v0.1647 TRIO Zornitza Stark Phenotypes for gene: TRIO were changed from to Mental retardation, autosomal dominant 44, MIM# 617061
Mendeliome v0.1646 TRIO Zornitza Stark Publications for gene: TRIO were set to
Mendeliome v0.1645 TRIO Zornitza Stark Mode of inheritance for gene: TRIO was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1644 TRIO Zornitza Stark reviewed gene: TRIO: Rating: GREEN; Mode of pathogenicity: None; Publications: 26721934, 32109419; Phenotypes: Mental retardation, autosomal dominant 44, MIM# 617061; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Microcephaly v0.92 TRIO Zornitza Stark Marked gene: TRIO as ready
Microcephaly v0.92 TRIO Zornitza Stark Gene: trio has been classified as Green List (High Evidence).
Microcephaly v0.92 TRIO Zornitza Stark Phenotypes for gene: TRIO were changed from to Mental retardation, autosomal dominant 44, MIM# 617061
Microcephaly v0.91 TRIO Zornitza Stark Publications for gene: TRIO were set to
Microcephaly v0.90 TRIO Zornitza Stark Mode of inheritance for gene: TRIO was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2420 TRIO Zornitza Stark changed review comment from: The nonsense mutations are spread along the TRIO sequence, and affected individuals show variable neurodevelopmental phenotypes. In contrast, missense variants cluster into two mutational hotspots in the TRIO sequence, one in the seventh spectrin repeat and one in the RAC1-activating GEFD1.; to: The nonsense mutations are spread along the TRIO sequence, and affected individuals show variable neurodevelopmental phenotypes. In contrast, missense variants cluster into two mutational hotspots in the TRIO sequence, one in the seventh spectrin repeat and one in the RAC1-activating GEFD1. Individuals with a pathogenic variant in the seventh spectrin repeat have a more severe ID associated with macrocephaly than do most individuals with GEFD1 variants, who display milder ID and microcephaly.
Microcephaly v0.89 TRIO Zornitza Stark reviewed gene: TRIO: Rating: GREEN; Mode of pathogenicity: None; Publications: 26721934, 32109419; Phenotypes: Mental retardation, autosomal dominant 44, MIM# 617061; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2420 TRIO Zornitza Stark Marked gene: TRIO as ready
Intellectual disability syndromic and non-syndromic v0.2420 TRIO Zornitza Stark Gene: trio has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2420 TRIO Zornitza Stark Phenotypes for gene: TRIO were changed from to Mental retardation, autosomal dominant 44, MIM# 617061
Intellectual disability syndromic and non-syndromic v0.2419 TRIO Zornitza Stark Publications for gene: TRIO were set to
Intellectual disability syndromic and non-syndromic v0.2418 TRIO Zornitza Stark Mode of inheritance for gene: TRIO was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2417 TRIO Zornitza Stark reviewed gene: TRIO: Rating: GREEN; Mode of pathogenicity: None; Publications: 26721934, 32109419; Phenotypes: Mental retardation, autosomal dominant 44, MIM# 617061; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Long QT Syndrome v0.7 CALM3 Zornitza Stark Marked gene: CALM3 as ready
Long QT Syndrome v0.7 CALM3 Zornitza Stark Gene: calm3 has been classified as Green List (High Evidence).
Long QT Syndrome v0.7 CALM3 Zornitza Stark Classified gene: CALM3 as Green List (high evidence)
Long QT Syndrome v0.7 CALM3 Zornitza Stark Gene: calm3 has been classified as Green List (High Evidence).
Long QT Syndrome v0.6 CALM3 Zornitza Stark gene: CALM3 was added
gene: CALM3 was added to Long QT Syndrome. Sources: Expert list
Mode of inheritance for gene: CALM3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CALM3 were set to 25460178; 31454269
Phenotypes for gene: CALM3 were set to Long QT syndrome 16, MIM# 618782
Review for gene: CALM3 was set to GREEN
Added comment: Sources: Expert list
Catecholaminergic Polymorphic Ventricular Tachycardia v0.10 CALM3 Zornitza Stark Classified gene: CALM3 as Red List (low evidence)
Catecholaminergic Polymorphic Ventricular Tachycardia v0.10 CALM3 Zornitza Stark Gene: calm3 has been classified as Red List (Low Evidence).
Catecholaminergic Polymorphic Ventricular Tachycardia v0.9 CALM3 Zornitza Stark reviewed gene: CALM3: Rating: RED; Mode of pathogenicity: None; Publications: 27516456; Phenotypes: Ventricular tachycardia, catecholaminergic polymorphic 6 618782; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Catecholaminergic Polymorphic Ventricular Tachycardia v0.9 CALM3 Zornitza Stark Marked gene: CALM3 as ready
Catecholaminergic Polymorphic Ventricular Tachycardia v0.9 CALM3 Zornitza Stark Gene: calm3 has been classified as Green List (High Evidence).
Catecholaminergic Polymorphic Ventricular Tachycardia v0.9 CALM3 Zornitza Stark Phenotypes for gene: CALM3 were changed from to Ventricular tachycardia, catecholaminergic polymorphic 6, MIM# 618782
Catecholaminergic Polymorphic Ventricular Tachycardia v0.8 CALM3 Zornitza Stark Publications for gene: CALM3 were set to 31454269; 27516456
Catecholaminergic Polymorphic Ventricular Tachycardia v0.7 CALM3 Zornitza Stark Publications for gene: CALM3 were set to
Catecholaminergic Polymorphic Ventricular Tachycardia v0.6 CALM3 Zornitza Stark Mode of inheritance for gene: CALM3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Congenital Disorders of Glycosylation v0.40 MAN1B1 Zornitza Stark Marked gene: MAN1B1 as ready
Congenital Disorders of Glycosylation v0.40 MAN1B1 Zornitza Stark Gene: man1b1 has been classified as Green List (High Evidence).
Congenital Disorders of Glycosylation v0.40 MAN1B1 Zornitza Stark Phenotypes for gene: MAN1B1 were changed from to Mental retardation, autosomal recessive 15, MIM#614202
Congenital Disorders of Glycosylation v0.39 MAN1B1 Zornitza Stark Mode of inheritance for gene: MAN1B1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Congenital Disorders of Glycosylation v0.38 MAN1B1 Zornitza Stark reviewed gene: MAN1B1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Mental retardation, autosomal recessive 15, MIM#614202; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2417 MAN1B1 Zornitza Stark Marked gene: MAN1B1 as ready
Intellectual disability syndromic and non-syndromic v0.2417 MAN1B1 Zornitza Stark Gene: man1b1 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2417 MAN1B1 Zornitza Stark Phenotypes for gene: MAN1B1 were changed from to Mental retardation, autosomal recessive 15, MIM#614202
Intellectual disability syndromic and non-syndromic v0.2416 MAN1B1 Zornitza Stark Mode of inheritance for gene: MAN1B1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2415 MAN1B1 Zornitza Stark reviewed gene: MAN1B1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Mental retardation, autosomal recessive 15, MIM#614202; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1644 MAN1B1 Zornitza Stark Marked gene: MAN1B1 as ready
Mendeliome v0.1644 MAN1B1 Zornitza Stark Gene: man1b1 has been classified as Green List (High Evidence).
Mendeliome v0.1644 MAN1B1 Zornitza Stark Phenotypes for gene: MAN1B1 were changed from to Mental retardation, autosomal recessive 15, MIM#614202
Mendeliome v0.1643 MAN1B1 Zornitza Stark Publications for gene: MAN1B1 were set to
Mendeliome v0.1642 MAN1B1 Zornitza Stark Mode of inheritance for gene: MAN1B1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2415 KMT2C Zornitza Stark Marked gene: KMT2C as ready
Intellectual disability syndromic and non-syndromic v0.2415 KMT2C Zornitza Stark Gene: kmt2c has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2415 KMT2C Zornitza Stark Phenotypes for gene: KMT2C were changed from to Kleefstra syndrome 2, MIM#617768
Intellectual disability syndromic and non-syndromic v0.2414 KMT2C Zornitza Stark Mode of inheritance for gene: KMT2C was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2413 KMT2C Zornitza Stark reviewed gene: KMT2C: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Kleefstra syndrome 2, MIM#617768; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1641 KMT2C Zornitza Stark Marked gene: KMT2C as ready
Mendeliome v0.1641 KMT2C Zornitza Stark Gene: kmt2c has been classified as Green List (High Evidence).
Mendeliome v0.1641 KMT2C Zornitza Stark Phenotypes for gene: KMT2C were changed from to Kleefstra syndrome 2, MIM#617768
Mendeliome v0.1640 KMT2C Zornitza Stark Mode of inheritance for gene: KMT2C was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1639 GLRX5 Zornitza Stark Marked gene: GLRX5 as ready
Mendeliome v0.1639 GLRX5 Zornitza Stark Gene: glrx5 has been classified as Green List (High Evidence).
Mendeliome v0.1639 GLRX5 Zornitza Stark Phenotypes for gene: GLRX5 were changed from to Anemia, sideroblastic, 3, pyridoxine-refractory; Spasticity, childhood-onset, with hyperglycinemia
Mendeliome v0.1638 GLRX5 Zornitza Stark Mode of inheritance for gene: GLRX5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Polymicrogyria and Schizencephaly v0.33 BICD2 Zornitza Stark Marked gene: BICD2 as ready
Polymicrogyria and Schizencephaly v0.33 BICD2 Zornitza Stark Added comment: Comment when marking as ready: Mild polymicrogyria described in SMA, 2B.
Polymicrogyria and Schizencephaly v0.33 BICD2 Zornitza Stark Gene: bicd2 has been classified as Green List (High Evidence).
Polymicrogyria and Schizencephaly v0.33 BICD2 Zornitza Stark Phenotypes for gene: BICD2 were changed from to Spinal muscular atrophy, lower extremity-predominant, 2B. MIM: 618291
Polymicrogyria and Schizencephaly v0.32 BICD2 Zornitza Stark Publications for gene: BICD2 were set to
Polymicrogyria and Schizencephaly v0.31 BICD2 Zornitza Stark Mode of inheritance for gene: BICD2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary Spastic Paraplegia - paediatric v0.6 ACOX1 Bryony Thompson reviewed gene: ACOX1: Rating: RED; Mode of pathogenicity: None; Publications: 18536048; Phenotypes: Peroxisomal acyl-CoA oxidase deficiency MIM#264470; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary Spastic Paraplegia - paediatric v0.6 AAAS Bryony Thompson Marked gene: AAAS as ready
Hereditary Spastic Paraplegia - paediatric v0.6 AAAS Bryony Thompson Gene: aaas has been classified as Amber List (Moderate Evidence).
Hereditary Spastic Paraplegia - paediatric v0.6 AAAS Bryony Thompson Classified gene: AAAS as Amber List (moderate evidence)
Hereditary Spastic Paraplegia - paediatric v0.6 AAAS Bryony Thompson Gene: aaas has been classified as Amber List (Moderate Evidence).
Hereditary Spastic Paraplegia - adult onset v0.5 Bryony Thompson removed gene:AAAS from the panel
Hereditary Spastic Paraplegia - paediatric v0.5 AAAS Bryony Thompson gene: AAAS was added
gene: AAAS was added to Hereditary Spastic Paraplegia - paediatric_RMH. Sources: Expert list
Mode of inheritance for gene: AAAS was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: AAAS were set to 30381913
Phenotypes for gene: AAAS were set to Achalasia-addisonianism-alacrimia syndrome MIM#231550; complicated hereditary spastic paraplegia
Review for gene: AAAS was set to AMBER
Added comment: Two families reported with complicated HSP.
Sources: Expert list
Hereditary Spastic Paraplegia Superpanel v0.0 Bryony Thompson Added Panel Hereditary Spastic Paraplegia Superpanel
Set child panels to: Hereditary Spastic Paraplegia - adult onset_RMH; Hereditary Spastic Paraplegia - paediatric_RMH
Brain Calcification v0.14 JAM2 Zornitza Stark edited their review of gene: JAM2: Changed rating: GREEN
Catecholaminergic Polymorphic Ventricular Tachycardia v0.5 RYR2 Zornitza Stark Marked gene: RYR2 as ready
Catecholaminergic Polymorphic Ventricular Tachycardia v0.5 RYR2 Zornitza Stark Gene: ryr2 has been classified as Green List (High Evidence).
Catecholaminergic Polymorphic Ventricular Tachycardia v0.5 RYR2 Zornitza Stark Phenotypes for gene: RYR2 were changed from to Ventricular tachycardia, catecholaminergic polymorphic, 1 604772
Catecholaminergic Polymorphic Ventricular Tachycardia v0.4 RYR2 Zornitza Stark Mode of inheritance for gene: RYR2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Catecholaminergic Polymorphic Ventricular Tachycardia v0.3 RYR2 Ivan Macciocca reviewed gene: RYR2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Ventricular tachycardia, catecholaminergic polymorphic, 1 604772; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2413 NUP188 Zornitza Stark edited their review of gene: NUP188: Changed rating: AMBER
Intellectual disability syndromic and non-syndromic v0.2413 NUP188 Zornitza Stark changed review comment from: Two unrelated individuals with homozygous truncating variants in this gene reported, Sandestin et al 2019, plus another by Strauss et al 2018. Also note two papers reporting mono allelic variants and disparate phenotypes (CDH and mitral valve prolapse, respectively), Yates et al, Haskell et al.; to: Two unrelated individuals with homozygous truncating variants in this gene reported, Sandestig et al 2019 (died in early infancy), plus another by Strauss et al 2018. Also note two papers reporting mono allelic variants and disparate phenotypes (CDH and mitral valve prolapse, respectively), Yates et al, Haskell et al.
Intellectual disability syndromic and non-syndromic v0.2413 NUP188 Zornitza Stark edited their review of gene: NUP188: Changed publications: 32021605, 28726809
Mendeliome v0.1637 NUDT2 Zornitza Stark Marked gene: NUDT2 as ready
Mendeliome v0.1637 NUDT2 Zornitza Stark Gene: nudt2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1637 NUDT2 Zornitza Stark Classified gene: NUDT2 as Amber List (moderate evidence)
Mendeliome v0.1637 NUDT2 Zornitza Stark Gene: nudt2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1636 NUDT2 Zornitza Stark gene: NUDT2 was added
gene: NUDT2 was added to Mendeliome. Sources: Expert list
Mode of inheritance for gene: NUDT2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NUDT2 were set to 27431290; 30059600
Phenotypes for gene: NUDT2 were set to Muscular hypotonia; Global developmental delay; Intellectual disability
Review for gene: NUDT2 was set to AMBER
Added comment: 7 affected individuals from 4 Saudi families, with same homozygous truncating variant.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2413 NUDT2 Zornitza Stark Marked gene: NUDT2 as ready
Intellectual disability syndromic and non-syndromic v0.2413 NUDT2 Zornitza Stark Gene: nudt2 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2413 NUDT2 Zornitza Stark Classified gene: NUDT2 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2413 NUDT2 Zornitza Stark Gene: nudt2 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2412 NUDT2 Zornitza Stark gene: NUDT2 was added
gene: NUDT2 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: NUDT2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NUDT2 were set to 27431290; 30059600
Phenotypes for gene: NUDT2 were set to Muscular hypotonia; Global developmental delay; Intellectual disability
Review for gene: NUDT2 was set to AMBER
Added comment: 7 affected individuals from 4 Saudi families, with same homozygous truncating variant.
Sources: Expert list
Mendeliome v0.1635 BPTF Michelle Torres reviewed gene: BPTF: Rating: GREEN; Mode of pathogenicity: None; Publications: 28942966; Phenotypes: Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies AD; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Catecholaminergic Polymorphic Ventricular Tachycardia v0.3 CALM3 Ain Roesley changed review comment from: PMID: 31454269; 4 families including 1 consanguineous family. Functional studies indicate reduced calcium binding for Glu141Lys and Glu141Val; to: PMID: 31454269; 4 families including 1 consanguineous family with LQTS. Functional studies indicate reduced calcium binding for Glu141Lys and Glu141Val
Mendeliome v0.1635 SLC26A4 Elena Savva reviewed gene: SLC26A4: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 24599119; Phenotypes: Deafness, autosomal recessive 4, with enlarged vestibular aqueduct 600791, Pendred syndrome 274600; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1635 MAP3K7 Michelle Torres reviewed gene: MAP3K7: Rating: GREEN; Mode of pathogenicity: Other; Publications: 27426734, 27426733; Phenotypes: Cardiospondylocarpofacial syndrome 157800 AD, Frontometaphyseal dysplasia 2 617137 AD; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Catecholaminergic Polymorphic Ventricular Tachycardia v0.3 CALM3 Ain Roesley reviewed gene: CALM3: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 31454269; Phenotypes: Long QT syndrome 16 (MIM# 618782); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1635 MAN1B1 Elena Savva reviewed gene: MAN1B1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 24348268; Phenotypes: Mental retardation, autosomal recessive 15; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Mendeliome v0.1635 KMT2C Elena Savva reviewed gene: KMT2C: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Kleefstra syndrome 2; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Mendeliome v0.1635 GLRX5 Elena Savva reviewed gene: GLRX5: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Anemia, sideroblastic, 3, pyridoxine-refractory, Spasticity, childhood-onset, with hyperglycinemia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Polymicrogyria and Schizencephaly v0.30 BICD2 Elena Savva reviewed gene: BICD2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 28635954, 32057122; Phenotypes: Spinal muscular atrophy, lower extremity-predominant, 2A. MIM: 615290, Spinal muscular atrophy, lower extremity-predominant, 2B. MIM: 618291; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Intellectual disability syndromic and non-syndromic v0.2411 NPHP3 Zornitza Stark reviewed gene: NPHP3: Rating: GREEN; Mode of pathogenicity: None; Publications: 18371931; Phenotypes: Meckel syndrome 7, MIM# 267010; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1635 NKAP Zornitza Stark Marked gene: NKAP as ready
Mendeliome v0.1635 NKAP Zornitza Stark Gene: nkap has been classified as Green List (High Evidence).
Mendeliome v0.1635 NKAP Zornitza Stark Classified gene: NKAP as Green List (high evidence)
Mendeliome v0.1635 NKAP Zornitza Stark Gene: nkap has been classified as Green List (High Evidence).
Mendeliome v0.1634 NKAP Zornitza Stark gene: NKAP was added
gene: NKAP was added to Mendeliome. Sources: Expert list
Mode of inheritance for gene: NKAP was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: NKAP were set to 26358559; 26350204; 31587868
Phenotypes for gene: NKAP were set to Intellectual disability
Review for gene: NKAP was set to GREEN
gene: NKAP was marked as current diagnostic
Added comment: 10 males from 8 unrelated families with missense mutations in NKAP (on Xq24) Hypotonia and tall stature with Marfanoid habitus was predominant phenotype. One variant (NM_024528:c.988G>A / p.Arg333Gln)
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2411 NKAP Zornitza Stark Marked gene: NKAP as ready
Intellectual disability syndromic and non-syndromic v0.2411 NKAP Zornitza Stark Gene: nkap has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2411 NKAP Zornitza Stark Classified gene: NKAP as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2411 NKAP Zornitza Stark Gene: nkap has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2410 NKAP Zornitza Stark gene: NKAP was added
gene: NKAP was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: NKAP was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Publications for gene: NKAP were set to 26358559; 26350204; 31587868
Phenotypes for gene: NKAP were set to Intellectual disability
Review for gene: NKAP was set to GREEN
gene: NKAP was marked as current diagnostic
Added comment: 10 males from 8 unrelated families with missense variants in NKAP. Main features: intellectual disability, hypotonia, tall stature with Marfanoid habitus. Recurrent variant (NM_024528:c.988G>A / p.Arg333Gln) seen in several families from different ethnic backgrounds.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2409 NHP2 Zornitza Stark Marked gene: NHP2 as ready
Intellectual disability syndromic and non-syndromic v0.2409 NHP2 Zornitza Stark Gene: nhp2 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2409 NHP2 Zornitza Stark Phenotypes for gene: NHP2 were changed from to Dyskeratosis congenita, autosomal recessive 2, MIM# 613987; Høyeraal-Hreidarsson syndrome
Intellectual disability syndromic and non-syndromic v0.2408 NHP2 Zornitza Stark Publications for gene: NHP2 were set to
Intellectual disability syndromic and non-syndromic v0.2407 NHP2 Zornitza Stark Mode of inheritance for gene: NHP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2406 NHP2 Zornitza Stark Classified gene: NHP2 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2406 NHP2 Zornitza Stark Gene: nhp2 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2405 NHP2 Zornitza Stark reviewed gene: NHP2: Rating: AMBER; Mode of pathogenicity: None; Publications: 18523010, 31985013; Phenotypes: Dyskeratosis congenita, autosomal recessive 2, MIM# 613987, Høyeraal-Hreidarsson syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2405 NHEJ1 Zornitza Stark Marked gene: NHEJ1 as ready
Intellectual disability syndromic and non-syndromic v0.2405 NHEJ1 Zornitza Stark Gene: nhej1 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2405 NHEJ1 Zornitza Stark Phenotypes for gene: NHEJ1 were changed from to Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation, MIM#611291
Intellectual disability syndromic and non-syndromic v0.2404 NHEJ1 Zornitza Stark Publications for gene: NHEJ1 were set to
Intellectual disability syndromic and non-syndromic v0.2403 NHEJ1 Zornitza Stark Mode of inheritance for gene: NHEJ1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2402 NHEJ1 Zornitza Stark Classified gene: NHEJ1 as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2402 NHEJ1 Zornitza Stark Gene: nhej1 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2401 NHEJ1 Zornitza Stark reviewed gene: NHEJ1: Rating: RED; Mode of pathogenicity: None; Publications: 16439204; Phenotypes: Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation, MIM#611291; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2401 NGF Zornitza Stark Marked gene: NGF as ready
Intellectual disability syndromic and non-syndromic v0.2401 NGF Zornitza Stark Gene: ngf has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2401 NGF Zornitza Stark Phenotypes for gene: NGF were changed from to Neuropathy, hereditary sensory and autonomic, type V, MIM# 608654
Intellectual disability syndromic and non-syndromic v0.2400 NGF Zornitza Stark Mode of inheritance for gene: NGF was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2399 NGF Zornitza Stark Classified gene: NGF as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2399 NGF Zornitza Stark Gene: ngf has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2398 NGF Zornitza Stark reviewed gene: NGF: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Neuropathy, hereditary sensory and autonomic, type V, MIM# 608654; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2398 NDUFV2 Zornitza Stark Classified gene: NDUFV2 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2398 NDUFV2 Zornitza Stark Gene: ndufv2 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2397 NDUFV2 Zornitza Stark changed review comment from: Multiple unrelated families.; to: Multiple unrelated families. Common presenting features include HOCM and encephalopathy, unclear in what proportion ID is likely to be the presenting or main feature.
Intellectual disability syndromic and non-syndromic v0.2397 NDUFV2 Zornitza Stark edited their review of gene: NDUFV2: Changed rating: AMBER
Intellectual disability syndromic and non-syndromic v0.2397 NDUFS6 Zornitza Stark Classified gene: NDUFS6 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2397 NDUFS6 Zornitza Stark Gene: ndufs6 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2396 NDUFS6 Zornitza Stark changed review comment from: Multiple affected families, functional data.; to: Multiple affected families, functional data. Limited clinical information in some reports. In some families, the presentation has been with severe neonatal lactic acidosis, therefore difficult to be sure in what proportion ID is likely to be the presenting or main feature.
Intellectual disability syndromic and non-syndromic v0.2396 NDUFS6 Zornitza Stark edited their review of gene: NDUFS6: Changed rating: AMBER
Intellectual disability syndromic and non-syndromic v0.2396 NDUFS3 Zornitza Stark Classified gene: NDUFS3 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2396 NDUFS3 Zornitza Stark Gene: ndufs3 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2395 NDUFS3 Zornitza Stark changed review comment from: At least three families reported.; to: At least three families reported. In the original report, the affected individual was phenotypically normal until 9 years of age but had rapidly progressive multi-system disease.
Intellectual disability syndromic and non-syndromic v0.2395 NDUFS3 Zornitza Stark edited their review of gene: NDUFS3: Changed rating: AMBER
Intellectual disability syndromic and non-syndromic v0.2395 NDUFS2 Zornitza Stark Classified gene: NDUFS2 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2395 NDUFS2 Zornitza Stark Gene: ndufs2 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2394 NDUFS2 Zornitza Stark changed review comment from: Multiple unrelated families. Phenotype in one family was more consistent with regression; in another family severe neonatal lactic acidosis led to death in the first few days of life; and in the third family presentation was with failure to thrive, vomiting, nystagmus, and specifically normal cognition despite delayed motor milestones due to hypotonia. Limited clinical information reported in other papers therefore difficult to know whether ID is likely to be the presenting or main feature of this mitochondrial disorder..; to: Multiple unrelated families. Phenotype in one family was more consistent with regression; in another family severe neonatal lactic acidosis led to death in the first few days of life; and in the third family presentation was with failure to thrive, vomiting, nystagmus, and specifically normal cognition despite delayed motor milestones due to hypotonia. Limited clinical information reported in other papers therefore difficult to know whether ID is likely to be the presenting or main feature of this mitochondrial disorder.
Intellectual disability syndromic and non-syndromic v0.2394 NDUFS2 Zornitza Stark changed review comment from: Multiple unrelated families.; to: Multiple unrelated families. Phenotype in one family was more consistent with regression; in another family severe neonatal lactic acidosis led to death in the first few days of life; and in the third family presentation was with failure to thrive, vomiting, nystagmus, and specifically normal cognition despite delayed motor milestones due to hypotonia. Limited clinical information reported in other papers therefore difficult to know whether ID is likely to be the presenting or main feature of this mitochondrial disorder..
Intellectual disability syndromic and non-syndromic v0.2394 NDUFS2 Zornitza Stark edited their review of gene: NDUFS2: Changed rating: AMBER
Callosome v0.104 TBR1 Zornitza Stark Marked gene: TBR1 as ready
Callosome v0.104 TBR1 Zornitza Stark Gene: tbr1 has been classified as Red List (Low Evidence).
Callosome v0.104 TBR1 Zornitza Stark Phenotypes for gene: TBR1 were changed from to Intellectual developmental disorder with autism and speech delay, MIM# 606053
Callosome v0.103 TBR1 Zornitza Stark Publications for gene: TBR1 were set to
Callosome v0.102 TBR1 Zornitza Stark Mode of inheritance for gene: TBR1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Callosome v0.101 TBR1 Zornitza Stark Classified gene: TBR1 as Red List (low evidence)
Callosome v0.101 TBR1 Zornitza Stark Gene: tbr1 has been classified as Red List (Low Evidence).
Callosome v0.100 TBR1 Zornitza Stark reviewed gene: TBR1: Rating: RED; Mode of pathogenicity: None; Publications: 25232744, 30250039; Phenotypes: Intellectual developmental disorder with autism and speech delay, MIM# 606053; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Autism v0.74 TBR1 Zornitza Stark Marked gene: TBR1 as ready
Autism v0.74 TBR1 Zornitza Stark Gene: tbr1 has been classified as Green List (High Evidence).
Autism v0.74 TBR1 Zornitza Stark Phenotypes for gene: TBR1 were changed from to Intellectual developmental disorder with autism and speech delay, MIM# 606053
Autism v0.73 TBR1 Zornitza Stark Publications for gene: TBR1 were set to
Autism v0.72 TBR1 Zornitza Stark Mode of inheritance for gene: TBR1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Autism v0.71 TBR1 Zornitza Stark reviewed gene: TBR1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25232744, 30250039; Phenotypes: Intellectual developmental disorder with autism and speech delay, MIM# 606053; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2394 TBR1 Zornitza Stark Marked gene: TBR1 as ready
Intellectual disability syndromic and non-syndromic v0.2394 TBR1 Zornitza Stark Gene: tbr1 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2394 TBR1 Zornitza Stark Phenotypes for gene: TBR1 were changed from to Intellectual developmental disorder with autism and speech delay, MIM# 606053
Intellectual disability syndromic and non-syndromic v0.2393 TBR1 Zornitza Stark Publications for gene: TBR1 were set to
Intellectual disability syndromic and non-syndromic v0.2392 TBR1 Zornitza Stark Mode of inheritance for gene: TBR1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2391 TBR1 Zornitza Stark reviewed gene: TBR1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25232744, 30250039; Phenotypes: Intellectual developmental disorder with autism and speech delay, MIM# 606053; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1633 TBR1 Zornitza Stark Marked gene: TBR1 as ready
Mendeliome v0.1633 TBR1 Zornitza Stark Gene: tbr1 has been classified as Green List (High Evidence).
Mendeliome v0.1633 TBR1 Zornitza Stark Phenotypes for gene: TBR1 were changed from to Intellectual developmental disorder with autism and speech delay, MIM# 606053
Mendeliome v0.1632 TBR1 Zornitza Stark Publications for gene: TBR1 were set to
Mendeliome v0.1631 TBR1 Zornitza Stark Mode of inheritance for gene: TBR1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Differences of Sex Development v0.14 GNRHR Zornitza Stark Marked gene: GNRHR as ready
Differences of Sex Development v0.14 GNRHR Zornitza Stark Gene: gnrhr has been classified as Green List (High Evidence).
Differences of Sex Development v0.14 GNRHR Zornitza Stark Phenotypes for gene: GNRHR were changed from to Hypogonadotropic hypogonadism 7 without anosmia, MIM#146110
Differences of Sex Development v0.13 GNRHR Zornitza Stark Publications for gene: GNRHR were set to
Differences of Sex Development v0.12 GNRHR Zornitza Stark Mode of inheritance for gene: GNRHR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Differences of Sex Development v0.11 GNRHR Zornitza Stark reviewed gene: GNRHR: Rating: GREEN; Mode of pathogenicity: None; Publications: 28348023, 9371856; Phenotypes: Hypogonadotropic hypogonadism 7 without anosmia, MIM#146110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1630 GNRHR Zornitza Stark Marked gene: GNRHR as ready
Mendeliome v0.1630 GNRHR Zornitza Stark Gene: gnrhr has been classified as Green List (High Evidence).
Mendeliome v0.1630 GNRHR Zornitza Stark Phenotypes for gene: GNRHR were changed from to Hypogonadotropic hypogonadism 7 without anosmia, MIM#146110
Mendeliome v0.1629 GNRHR Zornitza Stark Publications for gene: GNRHR were set to
Mendeliome v0.1628 GNRHR Zornitza Stark Mode of inheritance for gene: GNRHR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2391 NDUFS1 Zornitza Stark Marked gene: NDUFS1 as ready
Intellectual disability syndromic and non-syndromic v0.2391 NDUFS1 Zornitza Stark Gene: ndufs1 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2391 NDUFS1 Zornitza Stark Phenotypes for gene: NDUFS1 were changed from Mitochondrial complex I deficiency, nuclear type 5, MIM# 618226 to Mitochondrial complex I deficiency, nuclear type 5, MIM# 618226
Intellectual disability syndromic and non-syndromic v0.2390 NDUFS1 Zornitza Stark Phenotypes for gene: NDUFS1 were changed from to Mitochondrial complex I deficiency, nuclear type 5, MIM# 618226
Intellectual disability syndromic and non-syndromic v0.2390 NDUFS1 Zornitza Stark Publications for gene: NDUFS1 were set to 20382551
Intellectual disability syndromic and non-syndromic v0.2390 NDUFS1 Zornitza Stark Publications for gene: NDUFS1 were set to
Intellectual disability syndromic and non-syndromic v0.2389 NDUFS1 Zornitza Stark Mode of inheritance for gene: NDUFS1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2389 NDUFS1 Zornitza Stark Mode of inheritance for gene: NDUFS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2388 NDUFS1 Zornitza Stark reviewed gene: NDUFS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 20382551; Phenotypes: Mitochondrial complex I deficiency, nuclear type 5, MIM# 618226; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2388 NDUFB3 Zornitza Stark Classified gene: NDUFB3 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2388 NDUFB3 Zornitza Stark Gene: ndufb3 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2387 NDUFB3 Zornitza Stark changed review comment from: Ten families and functional data.; to: Ten families and functional data. In particular, the 8 families of shared Irish ancestry only had short stature and dysmorphic features, without marked metabolic disturbance. One of the other reported individuals died in infancy, again making it difficult to know whether ID would have been part of the phenotype.
Intellectual disability syndromic and non-syndromic v0.2387 NDUFB3 Zornitza Stark edited their review of gene: NDUFB3: Changed rating: AMBER
Intellectual disability syndromic and non-syndromic v0.2387 NDUFAF6 Zornitza Stark Classified gene: NDUFAF6 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2387 NDUFAF6 Zornitza Stark Gene: ndufaf6 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2386 NDUFAF6 Zornitza Stark changed review comment from: Multiple unrelated families reported.; to: Multiple unrelated families reported. Presentation in one family was with lactic acidosis in newborn period, and in another with regression in childhood. Limited phenotypic information for others. Unclear if and in what proportion of affected individuals ID is likely to be the main or presenting feature.
Intellectual disability syndromic and non-syndromic v0.2386 NDUFAF6 Zornitza Stark edited their review of gene: NDUFAF6: Changed rating: AMBER; Changed publications: 26741492, 18614015, 27623250
Intellectual disability syndromic and non-syndromic v0.2386 NDUFAF5 Zornitza Stark Marked gene: NDUFAF5 as ready
Intellectual disability syndromic and non-syndromic v0.2386 NDUFAF5 Zornitza Stark Gene: ndufaf5 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2386 NDUFAF5 Zornitza Stark Phenotypes for gene: NDUFAF5 were changed from to Mitochondrial complex I deficiency, nuclear type 16, MIM# 618238
Intellectual disability syndromic and non-syndromic v0.2385 NDUFAF5 Zornitza Stark Publications for gene: NDUFAF5 were set to
Intellectual disability syndromic and non-syndromic v0.2384 NDUFAF5 Zornitza Stark Mode of inheritance for gene: NDUFAF5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2383 NDUFAF5 Zornitza Stark Classified gene: NDUFAF5 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2383 NDUFAF5 Zornitza Stark Gene: ndufaf5 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2382 NDUFAF5 Zornitza Stark reviewed gene: NDUFAF5: Rating: AMBER; Mode of pathogenicity: None; Publications: 19542079, 21607760, 18940309; Phenotypes: Mitochondrial complex I deficiency, nuclear type 16, MIM# 618238; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2382 NDUFAF4 Zornitza Stark Classified gene: NDUFAF4 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2382 NDUFAF4 Zornitza Stark Gene: ndufaf4 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2381 NDUFAF4 Zornitza Stark changed review comment from: Two unrelated families and functional data.; to: Two unrelated families and functional data. Multiple affected individuals in one family (18179882) presented in newborn period with marked lactic acidosis, one long-term survivor (7yo at assessment) had profound ID. Individual from second family (28853723) presented in infancy with dev delay. Borderline gene-disease association for mitochondrial disease, and unclear what proportion of individuals are likely to present/manifest as ID.
Intellectual disability syndromic and non-syndromic v0.2381 NDUFAF4 Zornitza Stark edited their review of gene: NDUFAF4: Changed rating: AMBER
Intellectual disability syndromic and non-syndromic v0.2381 NDUFAF3 Zornitza Stark Classified gene: NDUFAF3 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2381 NDUFAF3 Zornitza Stark Gene: ndufaf3 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2380 NDUFAF3 Zornitza Stark changed review comment from: Three unrelated families reported.; to: Three unrelated families reported, severe neonatal presentation with lactic acidosis, seizures, and need for respiratory support. ID is unlikely to be the presenting or main feature.
Intellectual disability syndromic and non-syndromic v0.2380 NDUFAF3 Zornitza Stark edited their review of gene: NDUFAF3: Changed rating: AMBER
Intellectual disability syndromic and non-syndromic v0.2380 NDUFAF2 Zornitza Stark Classified gene: NDUFAF2 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2380 NDUFAF2 Zornitza Stark Gene: ndufaf2 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2379 NDUFAF2 Zornitza Stark changed review comment from: At least four unrelated families reported.; to: At least four unrelated families reported, complex neurological presentation with optic atrophy, nystagmus, ataxia in some, others described as ventilator-dependent. ID is unlikely to be the presenting or main feature.
Intellectual disability syndromic and non-syndromic v0.2379 NDUFAF2 Zornitza Stark edited their review of gene: NDUFAF2: Changed rating: AMBER
Intellectual disability syndromic and non-syndromic v0.2379 NDUFAF2 Zornitza Stark edited their review of gene: NDUFAF2: Changed publications: 20571988
Intellectual disability syndromic and non-syndromic v0.2379 NDUFAF1 Zornitza Stark changed review comment from: Three unrelated families described, DD/ID part of the phenotype.; to: Three unrelated families described, DD/ID part of the phenotype, specifically mentioned in two families, child in third family died in infancy from HOCM.
Intellectual disability syndromic and non-syndromic v0.2379 NDUFA9 Zornitza Stark Classified gene: NDUFA9 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2379 NDUFA9 Zornitza Stark Gene: ndufa9 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2378 NDUFA9 Zornitza Stark changed review comment from: Two unrelated families and functional data. Broad spectrum, likely to include ID.; to: Two unrelated families and functional data. Broad spectrum, likely to include ID but that is yet to be established.
Intellectual disability syndromic and non-syndromic v0.2378 NDUFA9 Zornitza Stark edited their review of gene: NDUFA9: Changed rating: AMBER
Mendeliome v0.1627 GNRHR Kristin Rigbye reviewed gene: GNRHR: Rating: GREEN; Mode of pathogenicity: None; Publications: 28348023, 9371856; Phenotypes: Hypogonadotropic hypogonadism 7 without anosmia, 146110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1627 TBR1 Melanie Marty reviewed gene: TBR1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25232744, 30250039; Phenotypes: Intellectual developmental disorder with autism and speech delay 606053; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2378 NDUFA10 Zornitza Stark Classified gene: NDUFA10 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2378 NDUFA10 Zornitza Stark Gene: ndufa10 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2377 NDUFA10 Zornitza Stark Deleted their comment
Intellectual disability syndromic and non-syndromic v0.2377 NDUFA10 Zornitza Stark edited their review of gene: NDUFA10: Added comment: Two families, functional data, but phenotypic description only available for one (DD/ID part of the phenotype).; Changed rating: AMBER
Mendeliome v0.1627 MYO9A Zornitza Stark Marked gene: MYO9A as ready
Mendeliome v0.1627 MYO9A Zornitza Stark Gene: myo9a has been classified as Green List (High Evidence).
Mendeliome v0.1627 MYO9A Zornitza Stark Phenotypes for gene: MYO9A were changed from to Congenital myasthenic syndrome 24, presynaptic, MIM# 618198
Mendeliome v0.1626 MYO9A Zornitza Stark Publications for gene: MYO9A were set to
Mendeliome v0.1625 MYO9A Zornitza Stark Mode of inheritance for gene: MYO9A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1624 MYO9A Zornitza Stark reviewed gene: MYO9A: Rating: GREEN; Mode of pathogenicity: None; Publications: 26752647, 27259756; Phenotypes: Congenital myasthenic syndrome 24, presynaptic, MIM# 618198; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital Myasthenia v0.20 MYO9A Zornitza Stark Publications for gene: MYO9A were set to 6752647; 27259756
Congenital Myasthenia v0.19 MYO9A Zornitza Stark Marked gene: MYO9A as ready
Congenital Myasthenia v0.19 MYO9A Zornitza Stark Gene: myo9a has been classified as Green List (High Evidence).
Congenital Myasthenia v0.19 MYO9A Zornitza Stark Phenotypes for gene: MYO9A were changed from congenital myasthenic syndrome 24, presynaptic 618198 to Congenital myasthenic syndrome 24, presynaptic 618198
Congenital Myasthenia v0.18 MYO9A Zornitza Stark Publications for gene: MYO9A were set to
Genetic Epilepsy v0.627 SYNGAP1 Zornitza Stark Marked gene: SYNGAP1 as ready
Genetic Epilepsy v0.627 SYNGAP1 Zornitza Stark Gene: syngap1 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.627 SYNGAP1 Zornitza Stark Phenotypes for gene: SYNGAP1 were changed from to Intellectual disability, autosomal dominant 5, MIM # 612621
Genetic Epilepsy v0.626 SYNGAP1 Zornitza Stark Publications for gene: SYNGAP1 were set to
Genetic Epilepsy v0.625 SYNGAP1 Zornitza Stark Mode of inheritance for gene: SYNGAP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Genetic Epilepsy v0.624 SYNGAP1 Zornitza Stark reviewed gene: SYNGAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26079862; Phenotypes: Intellectual disability, autosomal dominant 5, MIM # 612621; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2377 SYNGAP1 Zornitza Stark Marked gene: SYNGAP1 as ready
Intellectual disability syndromic and non-syndromic v0.2377 SYNGAP1 Zornitza Stark Gene: syngap1 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2377 SYNGAP1 Zornitza Stark Phenotypes for gene: SYNGAP1 were changed from to Intellectual disability, autosomal dominant 5 (MIM # 612621)
Intellectual disability syndromic and non-syndromic v0.2376 SYNGAP1 Zornitza Stark Publications for gene: SYNGAP1 were set to
Intellectual disability syndromic and non-syndromic v0.2375 SYNGAP1 Zornitza Stark Mode of inheritance for gene: SYNGAP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2374 NBN Zornitza Stark Marked gene: NBN as ready
Intellectual disability syndromic and non-syndromic v0.2374 NBN Zornitza Stark Gene: nbn has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2374 NBN Zornitza Stark Phenotypes for gene: NBN were changed from to Nijmegen breakage syndrome, MIM# 251260
Intellectual disability syndromic and non-syndromic v0.2373 NBN Zornitza Stark Mode of inheritance for gene: NBN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2372 NBN Zornitza Stark Classified gene: NBN as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2372 NBN Zornitza Stark Gene: nbn has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2371 NBN Zornitza Stark reviewed gene: NBN: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Nijmegen breakage syndrome, MIM# 251260; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2371 SYNGAP1 Ain Roesley reviewed gene: SYNGAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 26079862; Phenotypes: Intellectual disability, autosomal dominant 5 (MIM # 612621); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Vitreoretinopathy v0.2 Zornitza Stark Panel types changed to Victorian Clinical Genetics Services; Royal Melbourne Hospital; Rare Disease
Vitreoretinopathy v0.1 BEST1 Zornitza Stark Marked gene: BEST1 as ready
Vitreoretinopathy v0.1 BEST1 Zornitza Stark Gene: best1 has been classified as Green List (High Evidence).
Stickler Syndrome v0.2 Zornitza Stark Panel types changed to Victorian Clinical Genetics Services; Royal Melbourne Hospital; Rare Disease
Stickler Syndrome v0.1 LOXL3 Zornitza Stark Marked gene: LOXL3 as ready
Stickler Syndrome v0.1 LOXL3 Zornitza Stark Gene: loxl3 has been classified as Amber List (Moderate Evidence).
Stickler Syndrome v0.1 COL9A3 Zornitza Stark Marked gene: COL9A3 as ready
Stickler Syndrome v0.1 COL9A3 Zornitza Stark Gene: col9a3 has been classified as Green List (High Evidence).
Stickler Syndrome v0.0 LOXL3 Alison Yeung gene: LOXL3 was added
gene: LOXL3 was added to Stickler Syndrome. Sources: Expert list,Expert Review Amber
Mode of inheritance for gene: LOXL3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: LOXL3 were set to 30362103; 25663169
Phenotypes for gene: LOXL3 were set to Stickler syndrome
Vitreoretinopathy v0.0 ZNF408 Alison Yeung gene: ZNF408 was added
gene: ZNF408 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: ZNF408 was set to Unknown
Vitreoretinopathy v0.0 VCAN Alison Yeung gene: VCAN was added
gene: VCAN was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: VCAN was set to Unknown
Vitreoretinopathy v0.0 TSPAN12 Alison Yeung gene: TSPAN12 was added
gene: TSPAN12 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: TSPAN12 was set to Unknown
Vitreoretinopathy v0.0 NR2E3 Alison Yeung gene: NR2E3 was added
gene: NR2E3 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: NR2E3 was set to Unknown
Vitreoretinopathy v0.0 NDP Alison Yeung gene: NDP was added
gene: NDP was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: NDP was set to Unknown
Vitreoretinopathy v0.0 LRP5 Alison Yeung gene: LRP5 was added
gene: LRP5 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: LRP5 was set to Unknown
Vitreoretinopathy v0.0 KIF11 Alison Yeung gene: KIF11 was added
gene: KIF11 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: KIF11 was set to Unknown
Vitreoretinopathy v0.0 KCNJ13 Alison Yeung gene: KCNJ13 was added
gene: KCNJ13 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: KCNJ13 was set to Unknown
Stickler Syndrome v0.0 GZF1 Alison Yeung gene: GZF1 was added
gene: GZF1 was added to Stickler Syndrome. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: GZF1 was set to Unknown
Vitreoretinopathy v0.0 FZD4 Alison Yeung gene: FZD4 was added
gene: FZD4 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: FZD4 was set to Unknown
Vitreoretinopathy v0.0 CTNNB1 Alison Yeung gene: CTNNB1 was added
gene: CTNNB1 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: CTNNB1 was set to Unknown
Stickler Syndrome v0.0 COL9A3 Alison Yeung gene: COL9A3 was added
gene: COL9A3 was added to Stickler Syndrome. Sources: Expert Review Green,Other
Mode of inheritance for gene: COL9A3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: COL9A3 were set to 31090205; 30450842; 20301479; 24273071
Phenotypes for gene: COL9A3 were set to sensorineural hearing loss; midface hypoplasia; Stickler syndrome; myopia
Stickler Syndrome v0.0 COL9A2 Alison Yeung gene: COL9A2 was added
gene: COL9A2 was added to Stickler Syndrome. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: COL9A2 was set to Unknown
Stickler Syndrome v0.0 COL9A1 Alison Yeung gene: COL9A1 was added
gene: COL9A1 was added to Stickler Syndrome. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: COL9A1 was set to Unknown
Stickler Syndrome v0.0 COL2A1 Alison Yeung gene: COL2A1 was added
gene: COL2A1 was added to Stickler Syndrome. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: COL2A1 was set to Unknown
Vitreoretinopathy v0.0 COL18A1 Alison Yeung gene: COL18A1 was added
gene: COL18A1 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: COL18A1 was set to Unknown
Stickler Syndrome v0.0 COL11A2 Alison Yeung gene: COL11A2 was added
gene: COL11A2 was added to Stickler Syndrome. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: COL11A2 was set to Unknown
Stickler Syndrome v0.0 COL11A1 Alison Yeung gene: COL11A1 was added
gene: COL11A1 was added to Stickler Syndrome. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: COL11A1 was set to Unknown
Vitreoretinopathy v0.0 CAPN5 Alison Yeung gene: CAPN5 was added
gene: CAPN5 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: CAPN5 was set to Unknown
Vitreoretinopathy v0.0 BEST1 Alison Yeung gene: BEST1 was added
gene: BEST1 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: BEST1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: BEST1 were set to Vitreoretinochoroidopathy, MIM# 193220
Vitreoretinopathy v0.0 ATOH7 Alison Yeung gene: ATOH7 was added
gene: ATOH7 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: ATOH7 was set to Unknown
Stickler Syndrome v0.0 Alison Yeung Added panel Stickler Syndrome
Vitreoretinopathy v0.0 Alison Yeung Added panel Vitreoretinopathy
Mendeliome v0.1624 ZDHHC15 Zornitza Stark Marked gene: ZDHHC15 as ready
Mendeliome v0.1624 ZDHHC15 Zornitza Stark Gene: zdhhc15 has been classified as Red List (Low Evidence).
Mendeliome v0.1624 ZDHHC15 Zornitza Stark Phenotypes for gene: ZDHHC15 were changed from to Mental retardation, X-linked 91, 300577
Mendeliome v0.1623 ZDHHC15 Zornitza Stark Mode of inheritance for gene: ZDHHC15 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Mendeliome v0.1622 ZDHHC15 Zornitza Stark Classified gene: ZDHHC15 as Red List (low evidence)
Mendeliome v0.1622 ZDHHC15 Zornitza Stark Gene: zdhhc15 has been classified as Red List (Low Evidence).
Mendeliome v0.1621 ZDHHC15 Zornitza Stark reviewed gene: ZDHHC15: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Mental retardation, X-linked 91, 300577; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Intellectual disability syndromic and non-syndromic v0.2371 ZBTB24 Zornitza Stark Marked gene: ZBTB24 as ready
Intellectual disability syndromic and non-syndromic v0.2371 ZBTB24 Zornitza Stark Gene: zbtb24 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2371 ZBTB24 Zornitza Stark Phenotypes for gene: ZBTB24 were changed from to Immunodeficiency-centromeric instability-facial anomalies syndrome 2; OMIM # 614069
Intellectual disability syndromic and non-syndromic v0.2370 ZBTB24 Zornitza Stark Publications for gene: ZBTB24 were set to
Intellectual disability syndromic and non-syndromic v0.2369 ZBTB24 Zornitza Stark Mode of inheritance for gene: ZBTB24 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1621 ZBTB16 Zornitza Stark Marked gene: ZBTB16 as ready
Mendeliome v0.1621 ZBTB16 Zornitza Stark Gene: zbtb16 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1621 ZBTB16 Zornitza Stark Phenotypes for gene: ZBTB16 were changed from to Skeletal defects, genital hypoplasia, and mental retardation, OMIM #612447
Mendeliome v0.1620 ZBTB16 Zornitza Stark Publications for gene: ZBTB16 were set to
Mendeliome v0.1619 ZBTB16 Zornitza Stark Mode of inheritance for gene: ZBTB16 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1618 ZBTB16 Zornitza Stark Classified gene: ZBTB16 as Amber List (moderate evidence)
Mendeliome v0.1618 ZBTB16 Zornitza Stark Gene: zbtb16 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1617 ZBTB16 Zornitza Stark reviewed gene: ZBTB16: Rating: AMBER; Mode of pathogenicity: None; Publications: 18611983; Phenotypes: Skeletal defects, genital hypoplasia, and mental retardation, OMIM #612447; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2368 ZBTB16 Zornitza Stark Marked gene: ZBTB16 as ready
Intellectual disability syndromic and non-syndromic v0.2368 ZBTB16 Zornitza Stark Gene: zbtb16 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2368 ZBTB16 Zornitza Stark Phenotypes for gene: ZBTB16 were changed from to Skeletal defects, genital hypoplasia, and mental retardation, OMIM #612447
Intellectual disability syndromic and non-syndromic v0.2367 ZBTB16 Zornitza Stark Publications for gene: ZBTB16 were set to
Intellectual disability syndromic and non-syndromic v0.2366 ZBTB16 Zornitza Stark Mode of inheritance for gene: ZBTB16 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1617 ZBTB11 Zornitza Stark Marked gene: ZBTB11 as ready
Mendeliome v0.1617 ZBTB11 Zornitza Stark Gene: zbtb11 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1617 ZBTB11 Zornitza Stark Phenotypes for gene: ZBTB11 were changed from to Intellectual developmental disorder, autosomal recessive 69, OMIM #618383
Mendeliome v0.1616 ZBTB11 Zornitza Stark Publications for gene: ZBTB11 were set to
Mendeliome v0.1615 ZBTB11 Zornitza Stark Mode of inheritance for gene: ZBTB11 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1614 ZBTB11 Zornitza Stark Classified gene: ZBTB11 as Amber List (moderate evidence)
Mendeliome v0.1614 ZBTB11 Zornitza Stark Gene: zbtb11 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1613 ZBTB11 Zornitza Stark reviewed gene: ZBTB11: Rating: AMBER; Mode of pathogenicity: None; Publications: 29893856; Phenotypes: Intellectual developmental disorder, autosomal recessive 69, OMIM #618383; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2365 ZBTB11 Zornitza Stark Marked gene: ZBTB11 as ready
Intellectual disability syndromic and non-syndromic v0.2365 ZBTB11 Zornitza Stark Gene: zbtb11 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2365 ZBTB11 Zornitza Stark Phenotypes for gene: ZBTB11 were changed from to Intellectual developmental disorder, autosomal recessive 69; OMIM #618383
Intellectual disability syndromic and non-syndromic v0.2364 ZBTB11 Zornitza Stark Publications for gene: ZBTB11 were set to
Intellectual disability syndromic and non-syndromic v0.2363 ZBTB11 Zornitza Stark Mode of inheritance for gene: ZBTB11 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Anophthalmia_Microphthalmia_Coloboma v0.49 YAP1 Zornitza Stark Publications for gene: YAP1 were set to
Anophthalmia_Microphthalmia_Coloboma v0.48 YAP1 Zornitza Stark edited their review of gene: YAP1: Added comment: Four families reported; incomplete penetrance and variable expressivity.; Changed publications: 24462371, 27267789, 28801591
Intellectual disability syndromic and non-syndromic v0.2362 XPA Zornitza Stark Publications for gene: XPA were set to
Intellectual disability syndromic and non-syndromic v0.2361 XPA Zornitza Stark reviewed gene: XPA: Rating: GREEN; Mode of pathogenicity: None; Publications: 26302748, 25566891, 24135642; Phenotypes: Xeroderma pigmentosum, group A, OMIM# 278700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2361 WNT5A Zornitza Stark reviewed gene: WNT5A: Rating: GREEN; Mode of pathogenicity: None; Publications: 17256787; Phenotypes: Robinow syndrome, autosomal dominant 1, OMIM# 180700; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1613 WNT3 Zornitza Stark Marked gene: WNT3 as ready
Mendeliome v0.1613 WNT3 Zornitza Stark Gene: wnt3 has been classified as Red List (Low Evidence).
Mendeliome v0.1613 WNT3 Zornitza Stark Phenotypes for gene: WNT3 were changed from to Tetra-amelia syndrome 1, MIM# 273395
Mendeliome v0.1612 WNT3 Zornitza Stark Publications for gene: WNT3 were set to
Mendeliome v0.1611 WNT3 Zornitza Stark Mode of inheritance for gene: WNT3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1610 WNT3 Zornitza Stark Classified gene: WNT3 as Red List (low evidence)
Mendeliome v0.1610 WNT3 Zornitza Stark Gene: wnt3 has been classified as Red List (Low Evidence).
Mendeliome v0.1609 WNT3 Zornitza Stark reviewed gene: WNT3: Rating: RED; Mode of pathogenicity: None; Publications: 14872406; Phenotypes: Tetra-amelia syndrome 1, MIM# 273395; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Callosome v0.100 WNT3 Zornitza Stark Marked gene: WNT3 as ready
Callosome v0.100 WNT3 Zornitza Stark Gene: wnt3 has been classified as Red List (Low Evidence).
Callosome v0.100 WNT3 Zornitza Stark Phenotypes for gene: WNT3 were changed from to Tetra-amelia syndrome 1, MIM# 273395
Callosome v0.99 WNT3 Zornitza Stark Publications for gene: WNT3 were set to
Callosome v0.98 WNT3 Zornitza Stark Mode of inheritance for gene: WNT3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Callosome v0.97 WNT3 Zornitza Stark Classified gene: WNT3 as Red List (low evidence)
Callosome v0.97 WNT3 Zornitza Stark Gene: wnt3 has been classified as Red List (Low Evidence).
Callosome v0.96 WNT3 Zornitza Stark reviewed gene: WNT3: Rating: RED; Mode of pathogenicity: None; Publications: 14872406; Phenotypes: Tetra-amelia syndrome 1, MIM# 273395; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2361 WFS1 Zornitza Stark Phenotypes for gene: WFS1 were changed from to Wolfram syndrome 1, MIM# 222300; Wolfram-like syndrome, autosomal dominant, MIM# 614296
Intellectual disability syndromic and non-syndromic v0.2360 WFS1 Zornitza Stark Mode of inheritance for gene: WFS1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2359 WFS1 Zornitza Stark Classified gene: WFS1 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2359 WFS1 Zornitza Stark Gene: wfs1 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2358 WFS1 Zornitza Stark reviewed gene: WFS1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Wolfram syndrome 1, MIM# 222300, Wolfram-like syndrome, autosomal dominant, MIM# 614296; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Congenital Myasthenia v0.17 MYO9A Ain Roesley reviewed gene: MYO9A: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 26752647, 27259756; Phenotypes: Myasthenic syndrome, congenital, 24, presynaptic (MIM# 618198); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2358 WDR81 Zornitza Stark Marked gene: WDR81 as ready
Intellectual disability syndromic and non-syndromic v0.2358 WDR81 Zornitza Stark Gene: wdr81 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2358 WDR81 Zornitza Stark Phenotypes for gene: WDR81 were changed from to Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2, 610185; Hydrocephalus, congenital, 3, with brain anomalies, 617967
Intellectual disability syndromic and non-syndromic v0.2357 WDR81 Zornitza Stark Publications for gene: WDR81 were set to
Intellectual disability syndromic and non-syndromic v0.2356 WDR81 Zornitza Stark Mode of inheritance for gene: WDR81 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2355 WDR4 Zornitza Stark Marked gene: WDR4 as ready
Intellectual disability syndromic and non-syndromic v0.2355 WDR4 Zornitza Stark Added comment: Comment when marking as ready: Borderline Green rating: three families but two have the same homozygous variant; some functional data to support gene-disease association.
Intellectual disability syndromic and non-syndromic v0.2355 WDR4 Zornitza Stark Gene: wdr4 has been classified as Green List (High Evidence).
Regression v0.85 SPG11 Zornitza Stark Marked gene: SPG11 as ready
Regression v0.85 SPG11 Zornitza Stark Gene: spg11 has been classified as Green List (High Evidence).
Regression v0.85 SPG11 Zornitza Stark Classified gene: SPG11 as Green List (high evidence)
Regression v0.85 SPG11 Zornitza Stark Gene: spg11 has been classified as Green List (High Evidence).
Regression v0.84 SPG11 Zornitza Stark gene: SPG11 was added
gene: SPG11 was added to Regression. Sources: Expert Review
Mode of inheritance for gene: SPG11 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SPG11 were set to 21381113; 22554690; 19224311; 18067136; 27820618
Phenotypes for gene: SPG11 were set to Spastic paraplegia 11, autosomal recessive, MIM#604360; Charcot-Marie-Tooth disease, axonal, type 2X, MIM#616668; Amyotrophic lateral sclerosis 5, juvenile, MIM#602099
Review for gene: SPG11 was set to GREEN
gene: SPG11 was marked as current diagnostic
Added comment: Complex neurological phenotypes with onset in first and second decade, characterised by gradual deterioration.
Sources: Expert Review
Intellectual disability syndromic and non-syndromic v0.2355 WDR4 Zornitza Stark Marked gene: WDR4 as ready
Intellectual disability syndromic and non-syndromic v0.2355 WDR4 Zornitza Stark Gene: wdr4 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2355 WDR4 Zornitza Stark Publications for gene: WDR4 were set to PubMed: 26416026, 30079490, 29597095, 28617965
Mendeliome v0.1609 RS1 Zornitza Stark Marked gene: RS1 as ready
Mendeliome v0.1609 RS1 Zornitza Stark Gene: rs1 has been classified as Green List (High Evidence).
Mendeliome v0.1609 RS1 Zornitza Stark Phenotypes for gene: RS1 were changed from to Retinoschisis, MIM#312700
Mendeliome v0.1608 RS1 Zornitza Stark Publications for gene: RS1 were set to
Mendeliome v0.1607 RS1 Zornitza Stark Mode of inheritance for gene: RS1 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Hypertrichosis syndromes v0.9 SMC1A Zornitza Stark Marked gene: SMC1A as ready
Hypertrichosis syndromes v0.9 SMC1A Zornitza Stark Gene: smc1a has been classified as Green List (High Evidence).
Hypertrichosis syndromes v0.9 SMC1A Zornitza Stark Phenotypes for gene: SMC1A were changed from to Cornelia de Lange syndrome 2, MIM# 300590
Hypertrichosis syndromes v0.8 SMC1A Zornitza Stark Publications for gene: SMC1A were set to
Hypertrichosis syndromes v0.7 SMC1A Zornitza Stark Mode of inheritance for gene: SMC1A was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Hypertrichosis syndromes v0.6 SMC1A Zornitza Stark reviewed gene: SMC1A: Rating: GREEN; Mode of pathogenicity: None; Publications: 17273969, 22106055, 19701948, 26752331, 28166369; Phenotypes: Cornelia de Lange syndrome 2, MIM# 300590; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Mendeliome v0.1606 SMC1A Zornitza Stark Marked gene: SMC1A as ready
Mendeliome v0.1606 SMC1A Zornitza Stark Gene: smc1a has been classified as Green List (High Evidence).
Mendeliome v0.1606 SMC1A Zornitza Stark Phenotypes for gene: SMC1A were changed from to Cornelia de Lange syndrome 2, MIM# 300590
Mendeliome v0.1605 SMC1A Zornitza Stark Publications for gene: SMC1A were set to
Mendeliome v0.1604 SMC1A Zornitza Stark Mode of inheritance for gene: SMC1A was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Disorders of immune dysregulation v0.23 AIRE Zornitza Stark Marked gene: AIRE as ready
Disorders of immune dysregulation v0.23 AIRE Zornitza Stark Gene: aire has been classified as Green List (High Evidence).
Disorders of immune dysregulation v0.23 AIRE Zornitza Stark Phenotypes for gene: AIRE were changed from to Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia, MIM#240300
Disorders of immune dysregulation v0.22 AIRE Zornitza Stark Mode of inheritance for gene: AIRE was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Disorders of immune dysregulation v0.21 AIRE Zornitza Stark reviewed gene: AIRE: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia, MIM#240300; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mendeliome v0.1603 LOXHD1 Zornitza Stark Marked gene: LOXHD1 as ready
Mendeliome v0.1603 LOXHD1 Zornitza Stark Gene: loxhd1 has been classified as Green List (High Evidence).
Mendeliome v0.1603 AIRE Zornitza Stark Marked gene: AIRE as ready
Mendeliome v0.1603 AIRE Zornitza Stark Gene: aire has been classified as Green List (High Evidence).
Mendeliome v0.1603 AIRE Zornitza Stark Phenotypes for gene: AIRE were changed from to Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia, MIM#240300
Mendeliome v0.1602 AIRE Zornitza Stark Mode of pathogenicity for gene: AIRE was changed from to Other
Mendeliome v0.1601 AIRE Zornitza Stark Mode of inheritance for gene: AIRE was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mendeliome v0.1600 AIRE Zornitza Stark Mode of inheritance for gene: AIRE was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1599 LOXHD1 Zornitza Stark Phenotypes for gene: LOXHD1 were changed from to Deafness, autosomal recessive 77, MIM# 613079
Deafness_IsolatedAndComplex v0.328 LOXHD1 Zornitza Stark Marked gene: LOXHD1 as ready
Deafness_IsolatedAndComplex v0.328 LOXHD1 Zornitza Stark Gene: loxhd1 has been classified as Green List (High Evidence).
Mendeliome v0.1598 LOXHD1 Zornitza Stark Publications for gene: LOXHD1 were set to
Mendeliome v0.1597 LOXHD1 Zornitza Stark Mode of inheritance for gene: LOXHD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Deafness_IsolatedAndComplex v0.328 LOXHD1 Zornitza Stark Phenotypes for gene: LOXHD1 were changed from to Deafness, autosomal recessive 77, MIM# 613079
Mendeliome v0.1596 LOXHD1 Zornitza Stark reviewed gene: LOXHD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 19732867, 25792669; Phenotypes: Deafness, autosomal recessive 77, MIM# 613079; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Deafness_IsolatedAndComplex v0.327 LOXHD1 Zornitza Stark Publications for gene: LOXHD1 were set to
Deafness_IsolatedAndComplex v0.326 LOXHD1 Zornitza Stark Mode of inheritance for gene: LOXHD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1596 WFS1 Zornitza Stark Marked gene: WFS1 as ready
Mendeliome v0.1596 WFS1 Zornitza Stark Gene: wfs1 has been classified as Green List (High Evidence).
Mendeliome v0.1596 WFS1 Zornitza Stark Phenotypes for gene: WFS1 were changed from to ?Cataract 41; Deafness, autosomal dominant 6/14/38; Wolfram syndrome, autosomal recessive 1; Wolfram-like syndrome, autosomal dominant; {Diabetes mellitus, noninsulin-dependent, association with}
Mendeliome v0.1595 WFS1 Zornitza Stark Publications for gene: WFS1 were set to
Mendeliome v0.1594 WFS1 Zornitza Stark Mode of inheritance for gene: WFS1 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Arthrogryposis v0.25 PIEZO2 Zornitza Stark Marked gene: PIEZO2 as ready
Arthrogryposis v0.25 PIEZO2 Zornitza Stark Gene: piezo2 has been classified as Green List (High Evidence).
Arthrogryposis v0.25 PIEZO2 Zornitza Stark Phenotypes for gene: PIEZO2 were changed from to Arthrogryposis, distal, with impaired proprioception and touch (MIM # 617146)
Arthrogryposis v0.24 PIEZO2 Zornitza Stark Publications for gene: PIEZO2 were set to
Arthrogryposis v0.23 PIEZO2 Zornitza Stark Mode of inheritance for gene: PIEZO2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1593 ING3 Zornitza Stark Marked gene: ING3 as ready
Mendeliome v0.1593 ING3 Zornitza Stark Gene: ing3 has been classified as Red List (Low Evidence).
Mendeliome v0.1593 ING3 Zornitza Stark Classified gene: ING3 as Red List (low evidence)
Mendeliome v0.1593 ING3 Zornitza Stark Gene: ing3 has been classified as Red List (Low Evidence).
Mendeliome v0.1592 ING3 Zornitza Stark reviewed gene: ING3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Mendeliome v0.1592 SYN3 Zornitza Stark Marked gene: SYN3 as ready
Mendeliome v0.1592 SYN3 Zornitza Stark Gene: syn3 has been classified as Red List (Low Evidence).
Mendeliome v0.1592 SYN3 Zornitza Stark Classified gene: SYN3 as Red List (low evidence)
Mendeliome v0.1592 SYN3 Zornitza Stark Gene: syn3 has been classified as Red List (Low Evidence).
Mendeliome v0.1591 SYN3 Zornitza Stark reviewed gene: SYN3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Mendeliome v0.1591 SIM1 Zornitza Stark Marked gene: SIM1 as ready
Mendeliome v0.1591 SIM1 Zornitza Stark Gene: sim1 has been classified as Red List (Low Evidence).
Mendeliome v0.1591 SIM1 Zornitza Stark Classified gene: SIM1 as Red List (low evidence)
Mendeliome v0.1591 SIM1 Zornitza Stark Gene: sim1 has been classified as Red List (Low Evidence).
Mendeliome v0.1590 SIM1 Zornitza Stark reviewed gene: SIM1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Mendeliome v0.1590 RS1 Kristin Rigbye reviewed gene: RS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 15932525, 23453514, 23847049; Phenotypes: Retinoschisis, 312700; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Mendeliome v0.1590 SMC1A Melanie Marty reviewed gene: SMC1A: Rating: GREEN; Mode of pathogenicity: None; Publications: 17273969, 22106055, 19701948, 26752331, 28166369; Phenotypes: Cornelia de Lange syndrome 2 300590; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Deafness_IsolatedAndComplex v0.325 LOXHD1 Melanie Marty edited their review of gene: LOXHD1: Changed publications: 19732867, 25792669
Mendeliome v0.1590 AIRE Teresa Zhao reviewed gene: AIRE: Rating: GREEN; Mode of pathogenicity: Other; Publications: ; Phenotypes: Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Deafness_IsolatedAndComplex v0.325 LOXHD1 Melanie Marty reviewed gene: LOXHD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 19732867; Phenotypes: Deafness, autosomal recessive 77 613079; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1590 WFS1 Teresa Zhao reviewed gene: WFS1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 25211237; Phenotypes: ?Cataract 41, Deafness, autosomal dominant 6/14/38, Wolfram syndrome 1, Wolfram-like syndrome, autosomal dominant, {Diabetes mellitus, noninsulin-dependent, association with}; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Arthrogryposis v0.22 PIEZO2 Ain Roesley reviewed gene: PIEZO2: Rating: ; Mode of pathogenicity: None; Publications: PMID: 30941898; Phenotypes: Arthrogryposis, distal, with impaired proprioception and touch (MIM # 617146); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Bone Marrow Failure v0.43 Zornitza Stark removed gene:TCIRG1 from the panel
Genetic Epilepsy v0.624 VARS Zornitza Stark Marked gene: VARS as ready
Genetic Epilepsy v0.624 VARS Zornitza Stark Gene: vars has been classified as Green List (High Evidence).
Mendeliome v0.1590 VARS Zornitza Stark Publications for gene: VARS were set to
Mendeliome v0.1589 VARS Zornitza Stark Mode of inheritance for gene: VARS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Genetic Epilepsy v0.624 VARS Zornitza Stark Phenotypes for gene: VARS were changed from to Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy; OMIM #617802
Intellectual disability syndromic and non-syndromic v0.2354 VARS Zornitza Stark Marked gene: VARS as ready
Intellectual disability syndromic and non-syndromic v0.2354 VARS Zornitza Stark Gene: vars has been classified as Green List (High Evidence).
Genetic Epilepsy v0.623 VARS Zornitza Stark Publications for gene: VARS were set to
Mendeliome v0.1588 VARS Zornitza Stark reviewed gene: VARS: Rating: GREEN; Mode of pathogenicity: None; Publications: 30755616, 30755602, 26539891, 29691655, 30275004; Phenotypes: Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy, OMIM #617802; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genetic Epilepsy v0.622 VARS Zornitza Stark Mode of inheritance for gene: VARS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2354 VARS Zornitza Stark Publications for gene: VARS were set to PubMed: 30755616, 30755602, 26539891, 29691655, 30275004
Genetic Epilepsy v0.621 VARS Zornitza Stark reviewed gene: VARS: Rating: GREEN; Mode of pathogenicity: None; Publications: 30755616, 30755602, 26539891, 29691655, 30275004; Phenotypes: Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy, OMIM #617802; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Palmoplantar Keratoderma and Erythrokeratoderma v0.5 KRT6A Zornitza Stark Marked gene: KRT6A as ready
Palmoplantar Keratoderma and Erythrokeratoderma v0.5 KRT6A Zornitza Stark Gene: krt6a has been classified as Green List (High Evidence).
Palmoplantar Keratoderma and Erythrokeratoderma v0.5 KRT6A Zornitza Stark Phenotypes for gene: KRT6A were changed from to Pachyonychia congenita 3 (MIM#615726)
Palmoplantar Keratoderma and Erythrokeratoderma v0.4 KRT6A Zornitza Stark Publications for gene: KRT6A were set to
Palmoplantar Keratoderma and Erythrokeratoderma v0.3 KRT6A Zornitza Stark Mode of pathogenicity for gene: KRT6A was changed from to Other
Palmoplantar Keratoderma and Erythrokeratoderma v0.2 KRT6A Zornitza Stark Mode of inheritance for gene: KRT6A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1588 KRT6A Zornitza Stark Marked gene: KRT6A as ready
Mendeliome v0.1588 KRT6A Zornitza Stark Gene: krt6a has been classified as Green List (High Evidence).
Palmoplantar Keratoderma and Erythrokeratoderma v0.1 KRT6A Zornitza Stark reviewed gene: KRT6A: Rating: GREEN; Mode of pathogenicity: Other; Publications: 21326300; Phenotypes: Pachyonychia congenita 3 (MIM#615726); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1588 KRT6A Zornitza Stark Mode of pathogenicity for gene: KRT6A was changed from Other to Other
Mendeliome v0.1587 KRT6A Zornitza Stark Phenotypes for gene: KRT6A were changed from to Pachyonychia congenita 3 (MIM#615726)
Mendeliome v0.1586 KRT6A Zornitza Stark Publications for gene: KRT6A were set to
Mendeliome v0.1585 KRT6A Zornitza Stark Mode of pathogenicity for gene: KRT6A was changed from to Other
Mendeliome v0.1584 KRT6A Zornitza Stark Mode of inheritance for gene: KRT6A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Arthrogryposis v0.22 BICD2 Zornitza Stark Marked gene: BICD2 as ready
Arthrogryposis v0.22 BICD2 Zornitza Stark Added comment: Comment when marking as ready: Arthrogryposis is a feature in some affected individuals.
Arthrogryposis v0.22 BICD2 Zornitza Stark Gene: bicd2 has been classified as Green List (High Evidence).
Arthrogryposis v0.22 BICD2 Zornitza Stark Classified gene: BICD2 as Green List (high evidence)
Arthrogryposis v0.22 BICD2 Zornitza Stark Gene: bicd2 has been classified as Green List (High Evidence).
Arthrogryposis v0.21 BICD2 Elena Savva gene: BICD2 was added
gene: BICD2 was added to Arthrogryposis. Sources: Literature
Mode of inheritance for gene: BICD2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: BICD2 were set to PMID: 28635954; 27751653
Phenotypes for gene: BICD2 were set to Spinal muscular atrophy, lower extremity-predominant, 2A, autosomal dominant 615290; Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant 618291
Penetrance for gene: BICD2 were set to Incomplete
Review for gene: BICD2 was set to GREEN
Added comment: OMIM describes an established pathogenic variant (p.T703M) as inherited from an unaffected parent - has 2 hets in gnomAD

Requested for entry to this gene list following VPC - found several papers noting patient w/ Arthrogryposis
Sources: Literature
Intellectual disability syndromic and non-syndromic v0.2353 TXNL4A Zornitza Stark Marked gene: TXNL4A as ready
Intellectual disability syndromic and non-syndromic v0.2353 TXNL4A Zornitza Stark Gene: txnl4a has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2353 TXNL4A Zornitza Stark Phenotypes for gene: TXNL4A were changed from to Burn-McKeown syndrome, MIM# 608572
Intellectual disability syndromic and non-syndromic v0.2352 TXNL4A Zornitza Stark Mode of inheritance for gene: TXNL4A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2351 TXNL4A Zornitza Stark Classified gene: TXNL4A as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2351 TXNL4A Zornitza Stark Gene: txnl4a has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2350 TXNL4A Zornitza Stark reviewed gene: TXNL4A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Burn-McKeown syndrome, MIM# 608572; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2350 TUBGCP4 Zornitza Stark Marked gene: TUBGCP4 as ready
Intellectual disability syndromic and non-syndromic v0.2350 TUBGCP4 Zornitza Stark Gene: tubgcp4 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2350 TUBGCP4 Zornitza Stark Classified gene: TUBGCP4 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2350 TUBGCP4 Zornitza Stark Gene: tubgcp4 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2349 TUBGCP4 Zornitza Stark gene: TUBGCP4 was added
gene: TUBGCP4 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: TUBGCP4 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TUBGCP4 were set to 25817018
Phenotypes for gene: TUBGCP4 were set to Microcephaly and chorioretinopathy, autosomal recessive, 3, 616335
Review for gene: TUBGCP4 was set to AMBER
Added comment: Three unrelated families reported; ID described as mild.
Sources: Expert list
Callosome v0.96 TUBA8 Zornitza Stark Marked gene: TUBA8 as ready
Callosome v0.96 TUBA8 Zornitza Stark Gene: tuba8 has been classified as Red List (Low Evidence).
Callosome v0.96 TUBA8 Zornitza Stark Phenotypes for gene: TUBA8 were changed from to Cortical dysplasia, complex, with other brain malformations 8, MIM# 613180
Callosome v0.95 TUBA8 Zornitza Stark Publications for gene: TUBA8 were set to
Callosome v0.94 TUBA8 Zornitza Stark Mode of inheritance for gene: TUBA8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Callosome v0.93 TUBA8 Zornitza Stark Classified gene: TUBA8 as Red List (low evidence)
Callosome v0.93 TUBA8 Zornitza Stark Gene: tuba8 has been classified as Red List (Low Evidence).
Callosome v0.92 TUBA8 Zornitza Stark reviewed gene: TUBA8: Rating: RED; Mode of pathogenicity: None; Publications: 19896110, 31481326, 28388629; Phenotypes: Cortical dysplasia, complex, with other brain malformations 8, MIM# 613180; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genetic Epilepsy v0.621 TUBA8 Zornitza Stark Publications for gene: TUBA8 were set to 31481326; 19896110
Genetic Epilepsy v0.620 TUBA8 Zornitza Stark Classified gene: TUBA8 as Red List (low evidence)
Genetic Epilepsy v0.620 TUBA8 Zornitza Stark Gene: tuba8 has been classified as Red List (Low Evidence).
Genetic Epilepsy v0.619 TUBA8 Zornitza Stark edited their review of gene: TUBA8: Added comment: However, note that mouse model does not have a brain phenotype and WES in the original families identified homozygous, previously reported as pathogenic, LoF variant in SNAP29, which is much more likely to be causative (28388629).; Changed rating: RED; Changed publications: 31481326, 19896110, 28388629
Cerebellar and Pontocerebellar Hypoplasia v0.19 TUBA8 Zornitza Stark Marked gene: TUBA8 as ready
Cerebellar and Pontocerebellar Hypoplasia v0.19 TUBA8 Zornitza Stark Gene: tuba8 has been classified as Red List (Low Evidence).
Cerebellar and Pontocerebellar Hypoplasia v0.19 TUBA8 Zornitza Stark Phenotypes for gene: TUBA8 were changed from to Cortical dysplasia, complex, with other brain malformations 8, MIM# 613180
Mendeliome v0.1583 TUBA8 Zornitza Stark Marked gene: TUBA8 as ready
Mendeliome v0.1583 TUBA8 Zornitza Stark Gene: tuba8 has been classified as Red List (Low Evidence).
Mendeliome v0.1583 TUBA8 Zornitza Stark Phenotypes for gene: TUBA8 were changed from to Cortical dysplasia, complex, with other brain malformations 8, MIM# 613180
Mendeliome v0.1582 TUBA8 Zornitza Stark Publications for gene: TUBA8 were set to
Mendeliome v0.1581 TUBA8 Zornitza Stark Mode of inheritance for gene: TUBA8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Cerebellar and Pontocerebellar Hypoplasia v0.18 TUBA8 Zornitza Stark Publications for gene: TUBA8 were set to
Mendeliome v0.1580 TUBA8 Zornitza Stark Classified gene: TUBA8 as Red List (low evidence)
Mendeliome v0.1580 TUBA8 Zornitza Stark Gene: tuba8 has been classified as Red List (Low Evidence).
Cerebellar and Pontocerebellar Hypoplasia v0.17 TUBA8 Zornitza Stark Mode of inheritance for gene: TUBA8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Cerebellar and Pontocerebellar Hypoplasia v0.16 TUBA8 Zornitza Stark Classified gene: TUBA8 as Red List (low evidence)
Cerebellar and Pontocerebellar Hypoplasia v0.16 TUBA8 Zornitza Stark Gene: tuba8 has been classified as Red List (Low Evidence).
Mendeliome v0.1579 TUBA8 Zornitza Stark reviewed gene: TUBA8: Rating: RED; Mode of pathogenicity: None; Publications: 19896110, 31481326, 28388629; Phenotypes: Cortical dysplasia, complex, with other brain malformations 8, MIM# 613180; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cerebellar and Pontocerebellar Hypoplasia v0.15 TUBA8 Zornitza Stark reviewed gene: TUBA8: Rating: RED; Mode of pathogenicity: None; Publications: 19896110, 31481326, 28388629; Phenotypes: Cortical dysplasia, complex, with other brain malformations 8, MIM# 613180; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Tubulinopathies v0.6 TUBA8 Zornitza Stark Marked gene: TUBA8 as ready
Tubulinopathies v0.6 TUBA8 Zornitza Stark Gene: tuba8 has been classified as Red List (Low Evidence).
Tubulinopathies v0.6 TUBA8 Zornitza Stark Phenotypes for gene: TUBA8 were changed from to Cortical dysplasia, complex, with other brain malformations 8, MIM# 613180
Polymicrogyria and Schizencephaly v0.30 TUBA8 Zornitza Stark Phenotypes for gene: TUBA8 were changed from to Cortical dysplasia, complex, with other brain malformations 8, MIM# 613180
Polymicrogyria and Schizencephaly v0.29 TUBA8 Zornitza Stark Publications for gene: TUBA8 were set to
Polymicrogyria and Schizencephaly v0.28 TUBA8 Zornitza Stark Mode of inheritance for gene: TUBA8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Tubulinopathies v0.5 TUBA8 Zornitza Stark Publications for gene: TUBA8 were set to
Tubulinopathies v0.4 TUBA8 Zornitza Stark Mode of inheritance for gene: TUBA8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Tubulinopathies v0.3 TUBA8 Zornitza Stark Classified gene: TUBA8 as Red List (low evidence)
Tubulinopathies v0.3 TUBA8 Zornitza Stark Gene: tuba8 has been classified as Red List (Low Evidence).
Tubulinopathies v0.2 TUBA8 Zornitza Stark reviewed gene: TUBA8: Rating: RED; Mode of pathogenicity: None; Publications: 19896110, 31481326, 28388629; Phenotypes: Cortical dysplasia, complex, with other brain malformations 8, MIM# 613180; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Polymicrogyria and Schizencephaly v0.27 TUBA8 Zornitza Stark Classified gene: TUBA8 as Red List (low evidence)
Polymicrogyria and Schizencephaly v0.27 TUBA8 Zornitza Stark Gene: tuba8 has been classified as Red List (Low Evidence).
Polymicrogyria and Schizencephaly v0.26 TUBA8 Zornitza Stark reviewed gene: TUBA8: Rating: RED; Mode of pathogenicity: None; Publications: 19896110, 31481326, 28388629; Phenotypes: Cortical dysplasia, complex, with other brain malformations 8, MIM# 613180; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2348 TUBA8 Zornitza Stark Phenotypes for gene: TUBA8 were changed from to Cortical dysplasia, complex, with other brain malformations 8, MIM# 613180
Intellectual disability syndromic and non-syndromic v0.2347 TUBA8 Zornitza Stark Publications for gene: TUBA8 were set to
Intellectual disability syndromic and non-syndromic v0.2346 TUBA8 Zornitza Stark Mode of inheritance for gene: TUBA8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2345 TUBA8 Zornitza Stark Classified gene: TUBA8 as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2345 TUBA8 Zornitza Stark Gene: tuba8 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2344 TUBA8 Zornitza Stark reviewed gene: TUBA8: Rating: RED; Mode of pathogenicity: None; Publications: 19896110, 31481326, 28388629; Phenotypes: Cortical dysplasia, complex, with other brain malformations 8, MIM# 613180; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2344 TSHR Zornitza Stark Marked gene: TSHR as ready
Intellectual disability syndromic and non-syndromic v0.2344 TSHR Zornitza Stark Gene: tshr has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2344 TSHR Zornitza Stark Phenotypes for gene: TSHR were changed from to Hypothyroidism, congenital, nongoitrous, 1, MIM# 275200
Intellectual disability syndromic and non-syndromic v0.2343 TSHR Zornitza Stark Mode of inheritance for gene: TSHR was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2342 TSHR Zornitza Stark Mode of inheritance for gene: TSHR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2341 TSHR Zornitza Stark Classified gene: TSHR as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2341 TSHR Zornitza Stark Gene: tshr has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2340 TSHR Zornitza Stark reviewed gene: TSHR: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypothyroidism, congenital, nongoitrous, 1, MIM# 275200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2340 TSEN15 Zornitza Stark Marked gene: TSEN15 as ready
Intellectual disability syndromic and non-syndromic v0.2340 TSEN15 Zornitza Stark Gene: tsen15 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2340 TSEN15 Zornitza Stark Classified gene: TSEN15 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2340 TSEN15 Zornitza Stark Gene: tsen15 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2339 TSEN15 Zornitza Stark gene: TSEN15 was added
gene: TSEN15 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: TSEN15 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TSEN15 were set to 27392077; 30914295; 25558065
Phenotypes for gene: TSEN15 were set to Pontocerebellar hypoplasia, type 2F, 617026
Review for gene: TSEN15 was set to GREEN
Added comment: Three unrelated families reported.
Sources: Expert list
Bone Marrow Failure v0.41 VPS45 Zornitza Stark Marked gene: VPS45 as ready
Bone Marrow Failure v0.41 VPS45 Zornitza Stark Gene: vps45 has been classified as Green List (High Evidence).
Bone Marrow Failure v0.41 VPS45 Zornitza Stark Classified gene: VPS45 as Green List (high evidence)
Bone Marrow Failure v0.41 VPS45 Zornitza Stark Gene: vps45 has been classified as Green List (High Evidence).
Bone Marrow Failure v0.40 VPS45 Zornitza Stark gene: VPS45 was added
gene: VPS45 was added to Bone Marrow Failure. Sources: Expert list
Mode of inheritance for gene: VPS45 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: VPS45 were set to 23599270; 23738510
Phenotypes for gene: VPS45 were set to Neutropenia, severe congenital, 5, autosomal recessive, MIM#615285
Review for gene: VPS45 was set to GREEN
gene: VPS45 was marked as current diagnostic
Added comment: Same homozygous missense variant, p.Thr224Asn, identified in 6 Middle Eastern families. A different variant, p.Glu238Lys, identified in another family. Zebrafish model.
Sources: Expert list
Bone Marrow Failure v0.39 TCIRG1 Zornitza Stark Marked gene: TCIRG1 as ready
Bone Marrow Failure v0.39 TCIRG1 Zornitza Stark Gene: tcirg1 has been classified as Green List (High Evidence).
Bone Marrow Failure v0.39 TCIRG1 Zornitza Stark Classified gene: TCIRG1 as Green List (high evidence)
Bone Marrow Failure v0.39 TCIRG1 Zornitza Stark Gene: tcirg1 has been classified as Green List (High Evidence).
Bone Marrow Failure v0.38 TCIRG1 Zornitza Stark gene: TCIRG1 was added
gene: TCIRG1 was added to Bone Marrow Failure. Sources: Expert list
Mode of inheritance for gene: TCIRG1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: TCIRG1 were set to Osteopetrosis, autosomal recessive 1, MIM# 259700
Review for gene: TCIRG1 was set to GREEN
gene: TCIRG1 was marked as current diagnostic
Added comment: Pancytopaenia is a presenting feature.
Sources: Expert list
Radial Ray Abnormalities v0.8 RPL26 Zornitza Stark Marked gene: RPL26 as ready
Radial Ray Abnormalities v0.8 RPL26 Zornitza Stark Gene: rpl26 has been classified as Red List (Low Evidence).
Radial Ray Abnormalities v0.8 RPL26 Zornitza Stark Phenotypes for gene: RPL26 were changed from to Diamond-Blackfan anemia 11, MIM# 614900
Radial Ray Abnormalities v0.7 RPL26 Zornitza Stark Publications for gene: RPL26 were set to
Radial Ray Abnormalities v0.6 RPL26 Zornitza Stark Mode of inheritance for gene: RPL26 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Radial Ray Abnormalities v0.5 RPL26 Zornitza Stark Classified gene: RPL26 as Red List (low evidence)
Radial Ray Abnormalities v0.5 RPL26 Zornitza Stark Gene: rpl26 has been classified as Red List (Low Evidence).
Radial Ray Abnormalities v0.4 RPL26 Zornitza Stark reviewed gene: RPL26: Rating: RED; Mode of pathogenicity: None; Publications: 22431104; Phenotypes: Diamond-Blackfan anemia 11, MIM# 614900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1579 RPL26 Zornitza Stark Marked gene: RPL26 as ready
Mendeliome v0.1579 RPL26 Zornitza Stark Gene: rpl26 has been classified as Red List (Low Evidence).
Mendeliome v0.1579 RPL26 Zornitza Stark Phenotypes for gene: RPL26 were changed from to Diamond-Blackfan anemia 11, MIM# 614900
Mendeliome v0.1578 RPL26 Zornitza Stark Publications for gene: RPL26 were set to
Mendeliome v0.1577 RPL26 Zornitza Stark Mode of inheritance for gene: RPL26 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1576 RPL26 Zornitza Stark Classified gene: RPL26 as Red List (low evidence)
Mendeliome v0.1576 RPL26 Zornitza Stark Gene: rpl26 has been classified as Red List (Low Evidence).
Mendeliome v0.1575 RPL26 Zornitza Stark reviewed gene: RPL26: Rating: RED; Mode of pathogenicity: None; Publications: 22431104; Phenotypes: Diamond-Blackfan anemia 11, MIM# 614900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Diamond Blackfan anaemia v0.5 RPL26 Zornitza Stark Marked gene: RPL26 as ready
Diamond Blackfan anaemia v0.5 RPL26 Zornitza Stark Gene: rpl26 has been classified as Red List (Low Evidence).
Diamond Blackfan anaemia v0.5 RPL26 Zornitza Stark Phenotypes for gene: RPL26 were changed from to Diamond-Blackfan anemia 11, MIM# 614900
Diamond Blackfan anaemia v0.4 RPL26 Zornitza Stark Publications for gene: RPL26 were set to
Diamond Blackfan anaemia v0.3 RPL26 Zornitza Stark Mode of inheritance for gene: RPL26 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Diamond Blackfan anaemia v0.2 RPL26 Zornitza Stark Classified gene: RPL26 as Red List (low evidence)
Diamond Blackfan anaemia v0.2 RPL26 Zornitza Stark Gene: rpl26 has been classified as Red List (Low Evidence).
Diamond Blackfan anaemia v0.1 RPL26 Zornitza Stark reviewed gene: RPL26: Rating: RED; Mode of pathogenicity: None; Publications: 22431104; Phenotypes: Diamond-Blackfan anemia 11, MIM# 614900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Bone Marrow Failure v0.37 RPL26 Zornitza Stark Marked gene: RPL26 as ready
Bone Marrow Failure v0.37 RPL26 Zornitza Stark Gene: rpl26 has been classified as Red List (Low Evidence).
Bone Marrow Failure v0.37 RPL26 Zornitza Stark gene: RPL26 was added
gene: RPL26 was added to Bone Marrow Failure. Sources: Expert list
Mode of inheritance for gene: RPL26 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: RPL26 were set to 22431104
Phenotypes for gene: RPL26 were set to Diamond-Blackfan anemia 11, MIM# 614900
Review for gene: RPL26 was set to RED
Added comment: Single reported individual.
Sources: Expert list
Mendeliome v0.1575 KRT6A Crystle Lee reviewed gene: KRT6A: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID: 21326300; Phenotypes: Pachyonychia congenita 3 (MIM#615726); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Bone Marrow Failure v0.36 RPL15 Zornitza Stark Marked gene: RPL15 as ready
Bone Marrow Failure v0.36 RPL15 Zornitza Stark Gene: rpl15 has been classified as Green List (High Evidence).
Bone Marrow Failure v0.36 RPL15 Zornitza Stark Classified gene: RPL15 as Green List (high evidence)
Bone Marrow Failure v0.36 RPL15 Zornitza Stark Gene: rpl15 has been classified as Green List (High Evidence).
Bone Marrow Failure v0.35 RPL15 Zornitza Stark gene: RPL15 was added
gene: RPL15 was added to Bone Marrow Failure. Sources: Expert list
Mode of inheritance for gene: RPL15 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: RPL15 were set to 23812780; 29599205
Phenotypes for gene: RPL15 were set to Diamond-Blackfan anemia 12, MIM# 615550
Review for gene: RPL15 was set to GREEN
gene: RPL15 was marked as current diagnostic
Added comment: 7 unrelated individuals reported to date.
Sources: Expert list
Bone Marrow Failure v0.34 JAGN1 Zornitza Stark Marked gene: JAGN1 as ready
Bone Marrow Failure v0.34 JAGN1 Zornitza Stark Gene: jagn1 has been classified as Green List (High Evidence).
Bone Marrow Failure v0.34 JAGN1 Zornitza Stark Classified gene: JAGN1 as Green List (high evidence)
Bone Marrow Failure v0.34 JAGN1 Zornitza Stark Gene: jagn1 has been classified as Green List (High Evidence).
Bone Marrow Failure v0.33 JAGN1 Zornitza Stark gene: JAGN1 was added
gene: JAGN1 was added to Bone Marrow Failure. Sources: Expert list
Mode of inheritance for gene: JAGN1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: JAGN1 were set to 25129144
Phenotypes for gene: JAGN1 were set to Neutropenia, severe congenital, 6, autosomal recessive, MIM# 616022
Review for gene: JAGN1 was set to GREEN
gene: JAGN1 was marked as current diagnostic
Added comment: Fourteen individuals from 9 families reported.
Sources: Expert list
Bone Marrow Failure v0.32 ETV6 Zornitza Stark Marked gene: ETV6 as ready
Bone Marrow Failure v0.32 ETV6 Zornitza Stark Gene: etv6 has been classified as Green List (High Evidence).
Bone Marrow Failure v0.32 ETV6 Zornitza Stark Classified gene: ETV6 as Green List (high evidence)
Bone Marrow Failure v0.32 ETV6 Zornitza Stark Gene: etv6 has been classified as Green List (High Evidence).
Bone Marrow Failure v0.31 ETV6 Zornitza Stark gene: ETV6 was added
gene: ETV6 was added to Bone Marrow Failure. Sources: Expert list
Mode of inheritance for gene: ETV6 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: ETV6 were set to 25581430; 25807284
Phenotypes for gene: ETV6 were set to Thrombocytopenia 5, MIM# 616216
Review for gene: ETV6 was set to GREEN
gene: ETV6 was marked as current diagnostic
Added comment: At least 6 unrelated families reported.
Sources: Expert list
Bone Marrow Failure v0.30 CSF3R Zornitza Stark Marked gene: CSF3R as ready
Bone Marrow Failure v0.30 CSF3R Zornitza Stark Gene: csf3r has been classified as Green List (High Evidence).
Bone Marrow Failure v0.30 CSF3R Zornitza Stark Classified gene: CSF3R as Green List (high evidence)
Bone Marrow Failure v0.30 CSF3R Zornitza Stark Gene: csf3r has been classified as Green List (High Evidence).
Bone Marrow Failure v0.29 CSF3R Zornitza Stark gene: CSF3R was added
gene: CSF3R was added to Bone Marrow Failure. Sources: Expert list
Mode of inheritance for gene: CSF3R was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CSF3R were set to 24753537; 26324699
Phenotypes for gene: CSF3R were set to Neutropenia, severe congenital, 7, autosomal recessive, MIM# 617014
Review for gene: CSF3R was set to GREEN
gene: CSF3R was marked as current diagnostic
Added comment: Three unrelated families reported.
Sources: Expert list
Mendeliome v0.1575 ABCC6 Zornitza Stark Marked gene: ABCC6 as ready
Mendeliome v0.1575 ABCC6 Zornitza Stark Gene: abcc6 has been classified as Green List (High Evidence).
Mendeliome v0.1575 ABCC6 Zornitza Stark Phenotypes for gene: ABCC6 were changed from Pseudoxanthoma elasticum (MIM# 264800) to Pseudoxanthoma elasticum, MIM# 264800; Pseudoxanthoma elasticum, forme fruste, MIM#177850
Mendeliome v0.1574 ABCC6 Zornitza Stark Phenotypes for gene: ABCC6 were changed from to Pseudoxanthoma elasticum (MIM# 264800)
Mendeliome v0.1573 ABCC6 Zornitza Stark Publications for gene: ABCC6 were set to
Mendeliome v0.1572 ABCC6 Zornitza Stark Mode of inheritance for gene: ABCC6 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mendeliome v0.1571 ABCC6 Zornitza Stark Mode of inheritance for gene: ABCC6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Severe Combined Immunodeficiency (absent T present B cells) v0.9 PAX1 Zornitza Stark Marked gene: PAX1 as ready
Severe Combined Immunodeficiency (absent T present B cells) v0.9 PAX1 Zornitza Stark Gene: pax1 has been classified as Green List (High Evidence).
Severe Combined Immunodeficiency (absent T present B cells) v0.9 PAX1 Zornitza Stark Phenotypes for gene: PAX1 were changed from Syndromic SCID; dysmorphism; ear abnormalities; otofaciocervical syndrome to Syndromic SCID; dysmorphism; ear abnormalities; Otofaciocervical syndrome 2, MIM# 615560
Severe Combined Immunodeficiency (absent T present B cells) v0.8 PAX1 Zornitza Stark Classified gene: PAX1 as Green List (high evidence)
Severe Combined Immunodeficiency (absent T present B cells) v0.8 PAX1 Zornitza Stark Gene: pax1 has been classified as Green List (High Evidence).
Severe Combined Immunodeficiency (absent T present B cells) v0.7 PAX1 Zornitza Stark gene: PAX1 was added
gene: PAX1 was added to Severe Combined Immunodeficiency (absent T present B cells). Sources: Literature
Mode of inheritance for gene: PAX1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PAX1 were set to 32111619
Phenotypes for gene: PAX1 were set to Syndromic SCID; dysmorphism; ear abnormalities; otofaciocervical syndrome
Review for gene: PAX1 was set to GREEN
Added comment: 6 individuals from three unrelated families.
Sources: Literature
Mendeliome v0.1570 ABCC6 Ain Roesley reviewed gene: ABCC6: Rating: ; Mode of pathogenicity: None; Publications: PMID: 11536079; Phenotypes: Pseudoxanthoma elasticum (MIM# 264800); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2338 TRIP13 Zornitza Stark Marked gene: TRIP13 as ready
Intellectual disability syndromic and non-syndromic v0.2338 TRIP13 Zornitza Stark Gene: trip13 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2338 TRIP13 Zornitza Stark Phenotypes for gene: TRIP13 were changed from to Mosaic variegated aneuploidy syndrome 3, MIM# 617598
Intellectual disability syndromic and non-syndromic v0.2337 TRIP13 Zornitza Stark Publications for gene: TRIP13 were set to
Intellectual disability syndromic and non-syndromic v0.2336 TRIP13 Zornitza Stark Mode of inheritance for gene: TRIP13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2335 TRIP13 Zornitza Stark Classified gene: TRIP13 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2335 TRIP13 Zornitza Stark Gene: trip13 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2334 TRIP13 Zornitza Stark reviewed gene: TRIP13: Rating: AMBER; Mode of pathogenicity: None; Publications: 28553959; Phenotypes: Mosaic variegated aneuploidy syndrome 3, MIM# 617598; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1570 TRIM8 Zornitza Stark Marked gene: TRIM8 as ready
Mendeliome v0.1570 TRIM8 Zornitza Stark Gene: trim8 has been classified as Green List (High Evidence).
Mendeliome v0.1570 TRIM8 Zornitza Stark Phenotypes for gene: TRIM8 were changed from to Intellectual disability; Seizures
Mendeliome v0.1569 TRIM8 Zornitza Stark Publications for gene: TRIM8 were set to
Mendeliome v0.1568 TRIM8 Zornitza Stark Mode of inheritance for gene: TRIM8 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1567 TRIM8 Zornitza Stark reviewed gene: TRIM8: Rating: GREEN; Mode of pathogenicity: None; Publications: 30244534, 27346735, 23934111; Phenotypes: Intellectual disability, Seizures; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Genetic Epilepsy v0.619 TRIM8 Zornitza Stark Marked gene: TRIM8 as ready
Genetic Epilepsy v0.619 TRIM8 Zornitza Stark Gene: trim8 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.619 TRIM8 Zornitza Stark Phenotypes for gene: TRIM8 were changed from to Intellectual disability; Seizures
Genetic Epilepsy v0.618 TRIM8 Zornitza Stark Publications for gene: TRIM8 were set to
Genetic Epilepsy v0.617 TRIM8 Zornitza Stark Mode of inheritance for gene: TRIM8 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Genetic Epilepsy v0.616 TRIM8 Zornitza Stark reviewed gene: TRIM8: Rating: GREEN; Mode of pathogenicity: None; Publications: 30244534, 27346735, 23934111; Phenotypes: Intellectual disability, Seizures; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2334 TRIM8 Zornitza Stark changed review comment from: Six unrelated individuals reported.
Sources: Expert list; to: Six unrelated individuals reported. All variants reported to date are truncating, affecting the last (sixth exon) and as a result may escape nonsense-mediated decay. Since TRIM8 homodimerizes via its (upstream) coiled-coil domain and its C-terminal domain is required for nuclear localization, a dominant-negative effect is postulated by the authors. Haploinsufficiency appears less likely.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2334 TRIM8 Zornitza Stark Marked gene: TRIM8 as ready
Intellectual disability syndromic and non-syndromic v0.2334 TRIM8 Zornitza Stark Gene: trim8 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2334 TRIM8 Zornitza Stark Classified gene: TRIM8 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2334 TRIM8 Zornitza Stark Gene: trim8 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2333 TRIM8 Zornitza Stark gene: TRIM8 was added
gene: TRIM8 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: TRIM8 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: TRIM8 were set to 30244534; 27346735; 23934111
Phenotypes for gene: TRIM8 were set to Intellectual disability; Seizures
Review for gene: TRIM8 was set to GREEN
gene: TRIM8 was marked as current diagnostic
Added comment: Six unrelated individuals reported.
Sources: Expert list
Genetic Epilepsy v0.616 TRAK1 Zornitza Stark reviewed gene: TRAK1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28940097, 28364549, 29846532; Phenotypes: Epileptic encephalopathy, early infantile, 68, MIM# 618201; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2332 TRAK1 Zornitza Stark Marked gene: TRAK1 as ready
Intellectual disability syndromic and non-syndromic v0.2332 TRAK1 Zornitza Stark Gene: trak1 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2332 TRAK1 Zornitza Stark Phenotypes for gene: TRAK1 were changed from to Epileptic encephalopathy, early infantile, 68, MIM# 618201
Intellectual disability syndromic and non-syndromic v0.2331 TRAK1 Zornitza Stark Publications for gene: TRAK1 were set to
Intellectual disability syndromic and non-syndromic v0.2330 TRAK1 Zornitza Stark Mode of inheritance for gene: TRAK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2329 TRAK1 Zornitza Stark reviewed gene: TRAK1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28940097, 28364549, 29846532; Phenotypes: Epileptic encephalopathy, early infantile, 68, MIM# 618201; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2329 TRAIP Zornitza Stark Marked gene: TRAIP as ready
Intellectual disability syndromic and non-syndromic v0.2329 TRAIP Zornitza Stark Gene: traip has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2329 TRAIP Zornitza Stark Classified gene: TRAIP as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2329 TRAIP Zornitza Stark Gene: traip has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2328 TRAIP Zornitza Stark gene: TRAIP was added
gene: TRAIP was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: TRAIP was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: TRAIP were set to Seckel syndrome 9, MIM#616777
Review for gene: TRAIP was set to GREEN
gene: TRAIP was marked as current diagnostic
Added comment: Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2327 TPK1 Zornitza Stark Marked gene: TPK1 as ready
Intellectual disability syndromic and non-syndromic v0.2327 TPK1 Zornitza Stark Gene: tpk1 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2327 TPK1 Zornitza Stark Phenotypes for gene: TPK1 were changed from to Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type), MIM# 614458
Intellectual disability syndromic and non-syndromic v0.2326 TPK1 Zornitza Stark Mode of inheritance for gene: TPK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2325 TPK1 Zornitza Stark Classified gene: TPK1 as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2325 TPK1 Zornitza Stark Gene: tpk1 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2324 TPK1 Zornitza Stark reviewed gene: TPK1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type), MIM# 614458; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1567 TPH2 Zornitza Stark Marked gene: TPH2 as ready
Mendeliome v0.1567 TPH2 Zornitza Stark Gene: tph2 has been classified as Red List (Low Evidence).
Mendeliome v0.1567 TPH2 Zornitza Stark Phenotypes for gene: TPH2 were changed from to {Attention deficit-hyperactivity disorder, susceptibility to, 7} 613003
Mendeliome v0.1566 TPH2 Zornitza Stark Publications for gene: TPH2 were set to
Intellectual disability syndromic and non-syndromic v0.2324 TPH2 Zornitza Stark Marked gene: TPH2 as ready
Intellectual disability syndromic and non-syndromic v0.2324 TPH2 Zornitza Stark Gene: tph2 has been classified as Red List (Low Evidence).
Mendeliome v0.1565 TPH2 Zornitza Stark Mode of inheritance for gene: TPH2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1564 TPH2 Zornitza Stark Classified gene: TPH2 as Red List (low evidence)
Mendeliome v0.1564 TPH2 Zornitza Stark Gene: tph2 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2324 TPH2 Zornitza Stark Phenotypes for gene: TPH2 were changed from to {Attention deficit-hyperactivity disorder, susceptibility to, 7} 613003
Intellectual disability syndromic and non-syndromic v0.2323 TPH2 Zornitza Stark Publications for gene: TPH2 were set to
Mendeliome v0.1563 TPH2 Zornitza Stark reviewed gene: TPH2: Rating: RED; Mode of pathogenicity: None; Publications: 18347598; Phenotypes: {Attention deficit-hyperactivity disorder, susceptibility to, 7} 613003; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2322 TPH2 Zornitza Stark Mode of inheritance for gene: TPH2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2321 TPH2 Zornitza Stark Classified gene: TPH2 as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2321 TPH2 Zornitza Stark Gene: tph2 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2320 TPH2 Zornitza Stark reviewed gene: TPH2: Rating: RED; Mode of pathogenicity: None; Publications: 18347598; Phenotypes: {Attention deficit-hyperactivity disorder, susceptibility to, 7} 613003; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1563 SPOP Zornitza Stark Marked gene: SPOP as ready
Mendeliome v0.1563 SPOP Zornitza Stark Gene: spop has been classified as Green List (High Evidence).
Mendeliome v0.1563 SPOP Zornitza Stark Classified gene: SPOP as Green List (high evidence)
Mendeliome v0.1563 SPOP Zornitza Stark Gene: spop has been classified as Green List (High Evidence).
Mendeliome v0.1562 SPOP Zornitza Stark gene: SPOP was added
gene: SPOP was added to Mendeliome. Sources: Literature
Mode of inheritance for gene: SPOP was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SPOP were set to 32109420
Phenotypes for gene: SPOP were set to Intellectual disability; dysmorphism; microcephaly; macrocephaly
Mode of pathogenicity for gene: SPOP was set to Other
Review for gene: SPOP was set to GREEN
Added comment: Seven individuals reported with de novo missense variants in this gene. Gain-of-function variants associated with microcephaly whereas dominant-negative variants associated with macrocephaly.
Sources: Literature
Intellectual disability syndromic and non-syndromic v0.2320 SPOP Zornitza Stark Marked gene: SPOP as ready
Intellectual disability syndromic and non-syndromic v0.2320 SPOP Zornitza Stark Gene: spop has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2320 SPOP Zornitza Stark Classified gene: SPOP as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2320 SPOP Zornitza Stark Gene: spop has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2319 SPOP Zornitza Stark gene: SPOP was added
gene: SPOP was added to Intellectual disability syndromic and non-syndromic. Sources: Literature
Mode of inheritance for gene: SPOP was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SPOP were set to 32109420
Phenotypes for gene: SPOP were set to Intellectual disability; dysmorphism; microcephaly; macrocephaly
Mode of pathogenicity for gene: SPOP was set to Other
Review for gene: SPOP was set to GREEN
Added comment: Seven individuals reported with de novo missense variants in this gene. Gain-of-function variants associated with microcephaly whereas dominant-negative variants associated with macrocephaly.
Sources: Literature
Mendeliome v0.1561 TNIK Zornitza Stark Marked gene: TNIK as ready
Mendeliome v0.1561 TNIK Zornitza Stark Gene: tnik has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1561 TNIK Zornitza Stark Phenotypes for gene: TNIK were changed from to Mental retardation, autosomal recessive 54, MIM# 617028
Mendeliome v0.1560 TNIK Zornitza Stark Publications for gene: TNIK were set to
Mendeliome v0.1559 TNIK Zornitza Stark Mode of inheritance for gene: TNIK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1558 TNIK Zornitza Stark Classified gene: TNIK as Amber List (moderate evidence)
Mendeliome v0.1558 TNIK Zornitza Stark Gene: tnik has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1557 TNIK Zornitza Stark reviewed gene: TNIK: Rating: AMBER; Mode of pathogenicity: None; Publications: 27106596, 23035106; Phenotypes: Mental retardation, autosomal recessive 54, MIM# 617028; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2318 TNIK Zornitza Stark Marked gene: TNIK as ready
Intellectual disability syndromic and non-syndromic v0.2318 TNIK Zornitza Stark Gene: tnik has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2318 TNIK Zornitza Stark Phenotypes for gene: TNIK were changed from to Mental retardation, autosomal recessive 54, MIM# 617028
Intellectual disability syndromic and non-syndromic v0.2317 TNIK Zornitza Stark Publications for gene: TNIK were set to
Intellectual disability syndromic and non-syndromic v0.2316 TNIK Zornitza Stark Mode of inheritance for gene: TNIK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2315 TNIK Zornitza Stark Classified gene: TNIK as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2315 TNIK Zornitza Stark Gene: tnik has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2314 TNIK Zornitza Stark reviewed gene: TNIK: Rating: AMBER; Mode of pathogenicity: None; Publications: 27106596, 23035106; Phenotypes: Mental retardation, autosomal recessive 54, MIM# 617028; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Autism v0.71 TMLHE Zornitza Stark Classified gene: TMLHE as Green List (high evidence)
Autism v0.71 TMLHE Zornitza Stark Gene: tmlhe has been classified as Green List (High Evidence).
Autism v0.70 TMLHE Zornitza Stark gene: TMLHE was added
gene: TMLHE was added to Autism. Sources: Expert list
Mode of inheritance for gene: TMLHE was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Publications for gene: TMLHE were set to 21865298
Phenotypes for gene: TMLHE were set to {Autism, susceptibility to, X-linked 6}, MIM#300872
Review for gene: TMLHE was set to GREEN
Added comment: Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2314 TMLHE Zornitza Stark Marked gene: TMLHE as ready
Intellectual disability syndromic and non-syndromic v0.2314 TMLHE Zornitza Stark Gene: tmlhe has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2314 TMLHE Zornitza Stark Phenotypes for gene: TMLHE were changed from to {Autism, susceptibility to, X-linked 6} 300872
Mendeliome v0.1557 TMLHE Zornitza Stark Marked gene: TMLHE as ready
Mendeliome v0.1557 TMLHE Zornitza Stark Gene: tmlhe has been classified as Green List (High Evidence).
Mendeliome v0.1557 TMLHE Zornitza Stark Phenotypes for gene: TMLHE were changed from to {Autism, susceptibility to, X-linked 6}, MIM#300872
Mendeliome v0.1556 TMLHE Zornitza Stark Publications for gene: TMLHE were set to
Mendeliome v0.1555 TMLHE Zornitza Stark Mode of inheritance for gene: TMLHE was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Intellectual disability syndromic and non-syndromic v0.2313 TMLHE Zornitza Stark Publications for gene: TMLHE were set to 21865298
Mendeliome v0.1554 TMLHE Zornitza Stark reviewed gene: TMLHE: Rating: GREEN; Mode of pathogenicity: None; Publications: 21865298; Phenotypes: {Autism, susceptibility to, X-linked 6}, MIM#300872; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Intellectual disability syndromic and non-syndromic v0.2313 TMLHE Zornitza Stark Publications for gene: TMLHE were set to
Intellectual disability syndromic and non-syndromic v0.2312 TMLHE Zornitza Stark Mode of inheritance for gene: TMLHE was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Intellectual disability syndromic and non-syndromic v0.2311 TMLHE Zornitza Stark Classified gene: TMLHE as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2311 TMLHE Zornitza Stark Gene: tmlhe has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2310 TMLHE Zornitza Stark reviewed gene: TMLHE: Rating: AMBER; Mode of pathogenicity: None; Publications: 21865298; Phenotypes: {Autism, susceptibility to, X-linked 6} 300872; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Mendeliome v0.1554 TMEM94 Zornitza Stark Marked gene: TMEM94 as ready
Mendeliome v0.1554 TMEM94 Zornitza Stark Gene: tmem94 has been classified as Green List (High Evidence).
Mendeliome v0.1554 TMEM94 Zornitza Stark Classified gene: TMEM94 as Green List (high evidence)
Mendeliome v0.1554 TMEM94 Zornitza Stark Gene: tmem94 has been classified as Green List (High Evidence).
Mendeliome v0.1553 TMEM94 Zornitza Stark gene: TMEM94 was added
gene: TMEM94 was added to Mendeliome. Sources: Expert list
Mode of inheritance for gene: TMEM94 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TMEM94 were set to 30526868
Phenotypes for gene: TMEM94 were set to Intellectual developmental disorder with cardiac defects and dysmorphic facies, MIM#618316
Review for gene: TMEM94 was set to GREEN
Added comment: 10 individuals from 6 unrelated families.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2310 TMEM94 Zornitza Stark Marked gene: TMEM94 as ready
Intellectual disability syndromic and non-syndromic v0.2310 TMEM94 Zornitza Stark Gene: tmem94 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2310 TMEM94 Zornitza Stark Classified gene: TMEM94 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2310 TMEM94 Zornitza Stark Gene: tmem94 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2309 TMEM94 Zornitza Stark gene: TMEM94 was added
gene: TMEM94 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: TMEM94 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TMEM94 were set to 30526868
Phenotypes for gene: TMEM94 were set to Intellectual developmental disorder with cardiac defects and dysmorphic facies, MIM#618316
Review for gene: TMEM94 was set to GREEN
Added comment: 10 individuals from 6 unrelated families.
Sources: Expert list
Congenital Heart Defect v0.27 TMEM260 Zornitza Stark Marked gene: TMEM260 as ready
Congenital Heart Defect v0.27 TMEM260 Zornitza Stark Gene: tmem260 has been classified as Amber List (Moderate Evidence).
Congenital Heart Defect v0.27 TMEM260 Zornitza Stark Classified gene: TMEM260 as Amber List (moderate evidence)
Congenital Heart Defect v0.27 TMEM260 Zornitza Stark Gene: tmem260 has been classified as Amber List (Moderate Evidence).
Congenital Heart Defect v0.26 TMEM260 Zornitza Stark gene: TMEM260 was added
gene: TMEM260 was added to Congenital Heart Defect. Sources: Expert list
Mode of inheritance for gene: TMEM260 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TMEM260 were set to 28318500
Phenotypes for gene: TMEM260 were set to Structural heart defects and renal anomalies syndrome, MIM# 617478
Review for gene: TMEM260 was set to AMBER
Added comment: Two unrelated families with complex severe congenital heart disease.
Sources: Expert list
Mendeliome v0.1552 TMEM260 Zornitza Stark Marked gene: TMEM260 as ready
Mendeliome v0.1552 TMEM260 Zornitza Stark Gene: tmem260 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2308 TMEM260 Zornitza Stark Marked gene: TMEM260 as ready
Intellectual disability syndromic and non-syndromic v0.2308 TMEM260 Zornitza Stark Gene: tmem260 has been classified as Red List (Low Evidence).
Mendeliome v0.1552 TMEM260 Zornitza Stark Phenotypes for gene: TMEM260 were changed from to Structural heart defects and renal anomalies syndrome, MIM# 617478
Mendeliome v0.1551 TMEM260 Zornitza Stark Publications for gene: TMEM260 were set to
Intellectual disability syndromic and non-syndromic v0.2308 TMEM260 Zornitza Stark Phenotypes for gene: TMEM260 were changed from to Structural heart defects and renal anomalies syndrome, MIM# 617478
Mendeliome v0.1550 TMEM260 Zornitza Stark Mode of inheritance for gene: TMEM260 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1549 TMEM260 Zornitza Stark Classified gene: TMEM260 as Amber List (moderate evidence)
Mendeliome v0.1549 TMEM260 Zornitza Stark Gene: tmem260 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1548 TMEM260 Zornitza Stark reviewed gene: TMEM260: Rating: AMBER; Mode of pathogenicity: None; Publications: 28318500; Phenotypes: Structural heart defects and renal anomalies syndrome, MIM# 617478; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2307 TMEM260 Zornitza Stark Publications for gene: TMEM260 were set to
Intellectual disability syndromic and non-syndromic v0.2306 TMEM260 Zornitza Stark Mode of inheritance for gene: TMEM260 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2305 TMEM260 Zornitza Stark Classified gene: TMEM260 as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2305 TMEM260 Zornitza Stark Gene: tmem260 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2304 TMEM260 Zornitza Stark reviewed gene: TMEM260: Rating: RED; Mode of pathogenicity: None; Publications: 28318500; Phenotypes: Structural heart defects and renal anomalies syndrome, MIM# 617478; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1548 TKT Zornitza Stark Marked gene: TKT as ready
Mendeliome v0.1548 TKT Zornitza Stark Gene: tkt has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1548 TKT Zornitza Stark Phenotypes for gene: TKT were changed from to Short stature, developmental delay, and congenital heart defects; OMIM #617044
Mendeliome v0.1547 TKT Zornitza Stark Publications for gene: TKT were set to
Mendeliome v0.1546 TKT Zornitza Stark Mode of inheritance for gene: TKT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1545 TKT Zornitza Stark Classified gene: TKT as Amber List (moderate evidence)
Mendeliome v0.1545 TKT Zornitza Stark Gene: tkt has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1544 TKT Zornitza Stark reviewed gene: TKT: Rating: AMBER; Mode of pathogenicity: None; Publications: 27259054; Phenotypes: Short stature, developmental delay, and congenital heart defects, OMIM #617044; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2304 TKT Zornitza Stark Classified gene: TKT as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2304 TKT Zornitza Stark Gene: tkt has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2303 TKT Zornitza Stark reviewed gene: TKT: Rating: AMBER; Mode of pathogenicity: None; Publications: 27259054; Phenotypes: Short stature, developmental delay, and congenital heart defects, OMIM #617044; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2303 TINF2 Zornitza Stark Marked gene: TINF2 as ready
Intellectual disability syndromic and non-syndromic v0.2303 TINF2 Zornitza Stark Gene: tinf2 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2303 TINF2 Zornitza Stark Phenotypes for gene: TINF2 were changed from to Revesz syndrome, MIM# 268130
Intellectual disability syndromic and non-syndromic v0.2302 TINF2 Zornitza Stark Publications for gene: TINF2 were set to
Intellectual disability syndromic and non-syndromic v0.2301 TINF2 Zornitza Stark Mode of inheritance for gene: TINF2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2300 TINF2 Zornitza Stark reviewed gene: TINF2: Rating: GREEN; Mode of pathogenicity: None; Publications: 1404302, 18252230, 21477109; Phenotypes: Revesz syndrome, MIM# 268130; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability syndromic and non-syndromic v0.2300 TIMM50 Zornitza Stark Marked gene: TIMM50 as ready
Intellectual disability syndromic and non-syndromic v0.2300 TIMM50 Zornitza Stark Gene: timm50 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2300 TIMM50 Zornitza Stark Classified gene: TIMM50 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2300 TIMM50 Zornitza Stark Gene: timm50 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2299 TIMM50 Zornitza Stark gene: TIMM50 was added
gene: TIMM50 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: TIMM50 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TIMM50 were set to 27573165; 30190335; 31058414
Phenotypes for gene: TIMM50 were set to 3-methylglutaconic aciduria, type IX, MIM#617698
Review for gene: TIMM50 was set to GREEN
Added comment: Four unrelated families reported, ID is part of the phenotype.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2298 THRB Zornitza Stark changed review comment from: ID is not part of the phenotype.; to: ID is not generally part of the phenotype but a couple of more severe presentations including ID reported.
Intellectual disability syndromic and non-syndromic v0.2298 THRB Zornitza Stark edited their review of gene: THRB: Changed rating: AMBER; Changed publications: 22319036, 1682340
Intellectual disability syndromic and non-syndromic v0.2298 THRB Zornitza Stark Marked gene: THRB as ready
Intellectual disability syndromic and non-syndromic v0.2298 THRB Zornitza Stark Gene: thrb has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2298 THRB Zornitza Stark Phenotypes for gene: THRB were changed from to Thyroid hormone resistance, autosomal recessive, MIM# 274300; Thyroid hormone resistance, autosomal dominant, MIM# 188570
Intellectual disability syndromic and non-syndromic v0.2297 THRB Zornitza Stark Publications for gene: THRB were set to
Intellectual disability syndromic and non-syndromic v0.2296 THRB Zornitza Stark Mode of inheritance for gene: THRB was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2295 THRB Zornitza Stark Classified gene: THRB as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2295 THRB Zornitza Stark Gene: thrb has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2294 THRB Zornitza Stark Classified gene: THRB as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2294 THRB Zornitza Stark Gene: thrb has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2293 THRB Zornitza Stark reviewed gene: THRB: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Thyroid hormone resistance, autosomal recessive, MIM# 274300, Thyroid hormone resistance, autosomal dominant, MIM# 188570; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Inflammatory bowel disease v0.7 TGFB1 Zornitza Stark Marked gene: TGFB1 as ready
Inflammatory bowel disease v0.7 TGFB1 Zornitza Stark Gene: tgfb1 has been classified as Amber List (Moderate Evidence).
Inflammatory bowel disease v0.7 TGFB1 Zornitza Stark Classified gene: TGFB1 as Amber List (moderate evidence)
Inflammatory bowel disease v0.7 TGFB1 Zornitza Stark Gene: tgfb1 has been classified as Amber List (Moderate Evidence).
Inflammatory bowel disease v0.6 TGFB1 Zornitza Stark gene: TGFB1 was added
gene: TGFB1 was added to Inflammatory bowel disease. Sources: Expert list
Mode of inheritance for gene: TGFB1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TGFB1 were set to 29483653
Phenotypes for gene: TGFB1 were set to Inflammatory bowel disease, immunodeficiency, and encephalopathy, MIM# 618213
Review for gene: TGFB1 was set to AMBER
Added comment: Three individuals from two unrelated families reported. DD/ID and seizures in addition to IBD/immunodeficiency.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2293 TGFB1 Zornitza Stark Classified gene: TGFB1 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2293 TGFB1 Zornitza Stark Gene: tgfb1 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2292 TGFB1 Zornitza Stark gene: TGFB1 was added
gene: TGFB1 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: TGFB1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TGFB1 were set to 29483653
Phenotypes for gene: TGFB1 were set to Inflammatory bowel disease, immunodeficiency, and encephalopathy, MIM# 618213
Review for gene: TGFB1 was set to AMBER
Added comment: Three individuals from two unrelated families reported. DD/ID and seizures in addition to IBD/immunodeficiency.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2291 TERT Zornitza Stark reviewed gene: TERT: Rating: GREEN; Mode of pathogenicity: None; Publications: 18042801, 17785587; Phenotypes: Hoyeraal-Hreidarsson syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1544 TELO2 Zornitza Stark Marked gene: TELO2 as ready
Mendeliome v0.1544 TELO2 Zornitza Stark Gene: telo2 has been classified as Green List (High Evidence).
Mendeliome v0.1544 TELO2 Zornitza Stark Phenotypes for gene: TELO2 were changed from to You-Hoover-Fong syndrome, MIM#616954; Syndromic intellectual disability
Mendeliome v0.1543 TELO2 Zornitza Stark Publications for gene: TELO2 were set to
Mendeliome v0.1542 TELO2 Zornitza Stark Mode of inheritance for gene: TELO2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1541 TELO2 Zornitza Stark reviewed gene: TELO2: Rating: GREEN; Mode of pathogenicity: None; Publications: 27132593, 28944240; Phenotypes: You-Hoover-Fong syndrome, MIM#616954, Syndromic intellectual disability; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2291 TELO2 Zornitza Stark Marked gene: TELO2 as ready
Intellectual disability syndromic and non-syndromic v0.2291 TELO2 Zornitza Stark Gene: telo2 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2291 TELO2 Zornitza Stark Classified gene: TELO2 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2291 TELO2 Zornitza Stark Gene: telo2 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2290 TELO2 Zornitza Stark gene: TELO2 was added
gene: TELO2 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: TELO2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TELO2 were set to 27132593; 28944240
Phenotypes for gene: TELO2 were set to You-Hoover-Fong syndrome, MIM#616954; Syndromic intellectual disability
Review for gene: TELO2 was set to GREEN
Added comment: Five unrelated families reported.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2289 TECR Zornitza Stark Marked gene: TECR as ready
Intellectual disability syndromic and non-syndromic v0.2289 TECR Zornitza Stark Gene: tecr has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2289 TECR Zornitza Stark Phenotypes for gene: TECR were changed from to Mental retardation, autosomal recessive, MIM#614020
Intellectual disability syndromic and non-syndromic v0.2288 TECR Zornitza Stark Publications for gene: TECR were set to
Mendeliome v0.1541 TECR Zornitza Stark Marked gene: TECR as ready
Mendeliome v0.1541 TECR Zornitza Stark Gene: tecr has been classified as Red List (Low Evidence).
Mendeliome v0.1541 TECR Zornitza Stark Phenotypes for gene: TECR were changed from to Mental retardation, autosomal recessive, MIM#614020
Mendeliome v0.1540 TECR Zornitza Stark Publications for gene: TECR were set to
Mendeliome v0.1539 TECR Zornitza Stark Mode of inheritance for gene: TECR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1538 TECR Zornitza Stark Classified gene: TECR as Red List (low evidence)
Mendeliome v0.1538 TECR Zornitza Stark Gene: tecr has been classified as Red List (Low Evidence).
Mendeliome v0.1537 TECR Zornitza Stark reviewed gene: TECR: Rating: RED; Mode of pathogenicity: None; Publications: 21212097; Phenotypes: Mental retardation, autosomal recessive, MIM#614020; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2287 TECR Zornitza Stark Mode of inheritance for gene: TECR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2286 TECR Zornitza Stark Classified gene: TECR as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2286 TECR Zornitza Stark Gene: tecr has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2285 TECR Zornitza Stark reviewed gene: TECR: Rating: RED; Mode of pathogenicity: None; Publications: 21212097; Phenotypes: Mental retardation, autosomal recessive, MIM#614020; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1537 TBC1D7 Zornitza Stark Marked gene: TBC1D7 as ready
Mendeliome v0.1537 TBC1D7 Zornitza Stark Gene: tbc1d7 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1537 TBC1D7 Zornitza Stark Phenotypes for gene: TBC1D7 were changed from to Macrocephaly/megalencephaly syndrome, autosomal recessive, MIM# 248000
Mendeliome v0.1536 TBC1D7 Zornitza Stark Publications for gene: TBC1D7 were set to
Mendeliome v0.1535 TBC1D7 Zornitza Stark Mode of inheritance for gene: TBC1D7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1534 TBC1D7 Zornitza Stark Classified gene: TBC1D7 as Amber List (moderate evidence)
Mendeliome v0.1534 TBC1D7 Zornitza Stark Gene: tbc1d7 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1533 TBC1D7 Zornitza Stark reviewed gene: TBC1D7: Rating: AMBER; Mode of pathogenicity: None; Publications: 24515783, 23687350; Phenotypes: Macrocephaly/megalencephaly syndrome, autosomal recessive, MIM# 248000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Macrocephaly_Megalencephaly v0.31 TBC1D7 Zornitza Stark Marked gene: TBC1D7 as ready
Macrocephaly_Megalencephaly v0.31 TBC1D7 Zornitza Stark Gene: tbc1d7 has been classified as Amber List (Moderate Evidence).
Macrocephaly_Megalencephaly v0.31 TBC1D7 Zornitza Stark Phenotypes for gene: TBC1D7 were changed from to Macrocephaly/megalencephaly syndrome, autosomal recessive, MIM# 248000
Macrocephaly_Megalencephaly v0.30 TBC1D7 Zornitza Stark Publications for gene: TBC1D7 were set to
Macrocephaly_Megalencephaly v0.29 TBC1D7 Zornitza Stark Mode of inheritance for gene: TBC1D7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Macrocephaly_Megalencephaly v0.28 TBC1D7 Zornitza Stark Classified gene: TBC1D7 as Amber List (moderate evidence)
Macrocephaly_Megalencephaly v0.28 TBC1D7 Zornitza Stark Gene: tbc1d7 has been classified as Amber List (Moderate Evidence).
Macrocephaly_Megalencephaly v0.27 TBC1D7 Zornitza Stark reviewed gene: TBC1D7: Rating: AMBER; Mode of pathogenicity: None; Publications: 24515783, 23687350; Phenotypes: Macrocephaly/megalencephaly syndrome, autosomal recessive, MIM# 248000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2285 TBC1D7 Zornitza Stark Marked gene: TBC1D7 as ready
Intellectual disability syndromic and non-syndromic v0.2285 TBC1D7 Zornitza Stark Gene: tbc1d7 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2285 TBC1D7 Zornitza Stark Phenotypes for gene: TBC1D7 were changed from to Macrocephaly/megalencephaly syndrome, autosomal recessive, MIM# 248000
Intellectual disability syndromic and non-syndromic v0.2284 TBC1D7 Zornitza Stark Publications for gene: TBC1D7 were set to
Intellectual disability syndromic and non-syndromic v0.2283 TBC1D7 Zornitza Stark Mode of inheritance for gene: TBC1D7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2282 TBC1D7 Zornitza Stark Classified gene: TBC1D7 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2282 TBC1D7 Zornitza Stark Gene: tbc1d7 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2281 TBC1D7 Zornitza Stark reviewed gene: TBC1D7: Rating: AMBER; Mode of pathogenicity: None; Publications: 24515783, 23687350; Phenotypes: Macrocephaly/megalencephaly syndrome, autosomal recessive, MIM# 248000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2281 TASP1 Zornitza Stark changed review comment from: Four unrelated families reported; two with founder mutation. Protein interacts with KMT2A and KMT2D. Another infant with a de novo missense variant reported in a single infant with multiple congenital abnormalities, insufficient evidence for mono allelic disease at present.
Sources: Literature; to: Four unrelated families reported; two with founder mutation. Protein interacts with KMT2A and KMT2D. Another de novo missense variant reported in a single infant with multiple congenital abnormalities, insufficient evidence for mono allelic disease at present.
Sources: Literature
Microcephaly v0.89 TAF2 Zornitza Stark Marked gene: TAF2 as ready
Microcephaly v0.89 TAF2 Zornitza Stark Gene: taf2 has been classified as Amber List (Moderate Evidence).
Microcephaly v0.89 TAF2 Zornitza Stark Phenotypes for gene: TAF2 were changed from to Mental retardation, autosomal recessive 40, MIM# 615599
Microcephaly v0.88 TAF2 Zornitza Stark Publications for gene: TAF2 were set to
Microcephaly v0.87 TAF2 Zornitza Stark Mode of inheritance for gene: TAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Microcephaly v0.86 TAF2 Zornitza Stark Classified gene: TAF2 as Amber List (moderate evidence)
Microcephaly v0.86 TAF2 Zornitza Stark Gene: taf2 has been classified as Amber List (Moderate Evidence).
Microcephaly v0.85 TAF2 Zornitza Stark reviewed gene: TAF2: Rating: AMBER; Mode of pathogenicity: None; Publications: 21937992, 22633631, 26350204; Phenotypes: Mental retardation, autosomal recessive 40, MIM# 615599; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1533 TAF2 Zornitza Stark Marked gene: TAF2 as ready
Mendeliome v0.1533 TAF2 Zornitza Stark Gene: taf2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1533 TAF2 Zornitza Stark Phenotypes for gene: TAF2 were changed from to Mental retardation, autosomal recessive 40, MIM# 615599
Mendeliome v0.1532 TAF2 Zornitza Stark Publications for gene: TAF2 were set to
Mendeliome v0.1531 TAF2 Zornitza Stark Mode of inheritance for gene: TAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1530 TAF2 Zornitza Stark Classified gene: TAF2 as Amber List (moderate evidence)
Mendeliome v0.1530 TAF2 Zornitza Stark Gene: taf2 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1529 TAF2 Zornitza Stark reviewed gene: TAF2: Rating: AMBER; Mode of pathogenicity: None; Publications: 21937992, 22633631, 26350204; Phenotypes: Mental retardation, autosomal recessive 40, MIM# 615599; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2281 TAF2 Zornitza Stark Marked gene: TAF2 as ready
Intellectual disability syndromic and non-syndromic v0.2281 TAF2 Zornitza Stark Gene: taf2 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2281 TAF2 Zornitza Stark Phenotypes for gene: TAF2 were changed from to Mental retardation, autosomal recessive 40, MIM# 615599
Intellectual disability syndromic and non-syndromic v0.2280 TAF2 Zornitza Stark Publications for gene: TAF2 were set to
Intellectual disability syndromic and non-syndromic v0.2279 TAF2 Zornitza Stark Mode of inheritance for gene: TAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2278 TAF2 Zornitza Stark Classified gene: TAF2 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2278 TAF2 Zornitza Stark Gene: taf2 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2277 TAF2 Zornitza Stark reviewed gene: TAF2: Rating: AMBER; Mode of pathogenicity: None; Publications: 21937992, 22633631, 26350204; Phenotypes: Mental retardation, autosomal recessive 40, MIM# 615599; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1529 TAF13 Zornitza Stark Marked gene: TAF13 as ready
Mendeliome v0.1529 TAF13 Zornitza Stark Gene: taf13 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1529 TAF13 Zornitza Stark Phenotypes for gene: TAF13 were changed from to Mental retardation, autosomal recessive 60, MIM# 617432
Mendeliome v0.1528 TAF13 Zornitza Stark Publications for gene: TAF13 were set to
Mendeliome v0.1527 TAF13 Zornitza Stark Mode of inheritance for gene: TAF13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2277 TAF13 Zornitza Stark Marked gene: TAF13 as ready
Intellectual disability syndromic and non-syndromic v0.2277 TAF13 Zornitza Stark Gene: taf13 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2277 TAF13 Zornitza Stark Publications for gene: TAF13 were set to
Intellectual disability syndromic and non-syndromic v0.2276 TAF13 Zornitza Stark Phenotypes for gene: TAF13 were changed from to Mental retardation, autosomal recessive 60, MIM# 617432
Mendeliome v0.1526 TAF13 Zornitza Stark Classified gene: TAF13 as Amber List (moderate evidence)
Mendeliome v0.1526 TAF13 Zornitza Stark Gene: taf13 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.1525 TAF13 Zornitza Stark reviewed gene: TAF13: Rating: AMBER; Mode of pathogenicity: None; Publications: 28257693; Phenotypes: Mental retardation, autosomal recessive 60, MIM# 617432; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2275 TAF13 Zornitza Stark Mode of inheritance for gene: TAF13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2274 TAF13 Zornitza Stark Classified gene: TAF13 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2274 TAF13 Zornitza Stark Gene: taf13 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2273 TAF13 Zornitza Stark reviewed gene: TAF13: Rating: AMBER; Mode of pathogenicity: None; Publications: 28257693; Phenotypes: Mental retardation, autosomal recessive 60, MIM# 617432; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.108 TACO1 Zornitza Stark Marked gene: TACO1 as ready
Mitochondrial disease v0.108 TACO1 Zornitza Stark Gene: taco1 has been classified as Green List (High Evidence).
Mitochondrial disease v0.108 TACO1 Zornitza Stark Phenotypes for gene: TACO1 were changed from to Mitochondrial complex IV deficiency; OMIM #220110
Mitochondrial disease v0.107 TACO1 Zornitza Stark Publications for gene: TACO1 were set to
Mitochondrial disease v0.106 TACO1 Zornitza Stark Mode of inheritance for gene: TACO1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.105 TACO1 Zornitza Stark reviewed gene: TACO1: Rating: GREEN; Mode of pathogenicity: None; Publications: 19503089, 20727754, 25044680, 27319982; Phenotypes: Mitochondrial complex IV deficiency, OMIM #220110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Regression v0.83 SYT14 Zornitza Stark Marked gene: SYT14 as ready
Regression v0.83 SYT14 Zornitza Stark Gene: syt14 has been classified as Red List (Low Evidence).
Regression v0.83 SYT14 Zornitza Stark Phenotypes for gene: SYT14 were changed from to Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229
Regression v0.82 SYT14 Zornitza Stark Publications for gene: SYT14 were set to
Regression v0.81 SYT14 Zornitza Stark Mode of inheritance for gene: SYT14 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Regression v0.80 SYT14 Zornitza Stark Classified gene: SYT14 as Red List (low evidence)
Regression v0.80 SYT14 Zornitza Stark Gene: syt14 has been classified as Red List (Low Evidence).
Regression v0.79 SYT14 Zornitza Stark reviewed gene: SYT14: Rating: RED; Mode of pathogenicity: None; Publications: 21835308; Phenotypes: Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1525 SYT14 Zornitza Stark Marked gene: SYT14 as ready
Mendeliome v0.1525 SYT14 Zornitza Stark Gene: syt14 has been classified as Red List (Low Evidence).
Mendeliome v0.1525 SYT14 Zornitza Stark Phenotypes for gene: SYT14 were changed from to Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229
Mendeliome v0.1524 SYT14 Zornitza Stark Publications for gene: SYT14 were set to
Mendeliome v0.1523 SYT14 Zornitza Stark Mode of inheritance for gene: SYT14 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1522 SYT14 Zornitza Stark Classified gene: SYT14 as Red List (low evidence)
Mendeliome v0.1522 SYT14 Zornitza Stark Gene: syt14 has been classified as Red List (Low Evidence).
Mendeliome v0.1521 SYT14 Zornitza Stark reviewed gene: SYT14: Rating: RED; Mode of pathogenicity: None; Publications: 21835308; Phenotypes: Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2273 SYT14 Zornitza Stark Phenotypes for gene: SYT14 were changed from Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229 to Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229
Intellectual disability syndromic and non-syndromic v0.2272 SYT14 Zornitza Stark Marked gene: SYT14 as ready
Intellectual disability syndromic and non-syndromic v0.2272 SYT14 Zornitza Stark Gene: syt14 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2272 SYT14 Zornitza Stark Phenotypes for gene: SYT14 were changed from to Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229
Intellectual disability syndromic and non-syndromic v0.2271 SYT14 Zornitza Stark Publications for gene: SYT14 were set to
Intellectual disability syndromic and non-syndromic v0.2270 SYT14 Zornitza Stark Mode of inheritance for gene: SYT14 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2269 SYT14 Zornitza Stark Classified gene: SYT14 as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2269 SYT14 Zornitza Stark Gene: syt14 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2268 SYT14 Zornitza Stark reviewed gene: SYT14: Rating: RED; Mode of pathogenicity: None; Publications: 21835308; Phenotypes: Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2268 SUZ12 Zornitza Stark Phenotypes for gene: SUZ12 were changed from no OMIM number yet. to Imagawa-Matsumoto syndrome, MIM# 618786; Intellectual disability; Overgrowth
Intellectual disability syndromic and non-syndromic v0.2267 SUZ12 Zornitza Stark reviewed gene: SUZ12: Rating: GREEN; Mode of pathogenicity: None; Publications: 31736240, 30019515, 28229514; Phenotypes: Imagawa-Matsumoto syndrome, MIM# 618786, Intellectual disability, Overgrowth; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Ciliopathies v0.72 SUFU Zornitza Stark Marked gene: SUFU as ready
Ciliopathies v0.72 SUFU Zornitza Stark Gene: sufu has been classified as Amber List (Moderate Evidence).
Ciliopathies v0.72 SUFU Zornitza Stark Phenotypes for gene: SUFU were changed from to Joubert syndrome 32, MIM#617757
Ciliopathies v0.71 SUFU Zornitza Stark Publications for gene: SUFU were set to
Ciliopathies v0.70 SUFU Zornitza Stark Mode of inheritance for gene: SUFU was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Ciliopathies v0.69 SUFU Zornitza Stark Classified gene: SUFU as Amber List (moderate evidence)
Ciliopathies v0.69 SUFU Zornitza Stark Gene: sufu has been classified as Amber List (Moderate Evidence).
Ciliopathies v0.68 SUFU Zornitza Stark reviewed gene: SUFU: Rating: AMBER; Mode of pathogenicity: None; Publications: 28965847; Phenotypes: Joubert syndrome 32, MIM#617757; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Joubert syndrome and other neurological ciliopathies v0.20 SUFU Zornitza Stark Marked gene: SUFU as ready
Joubert syndrome and other neurological ciliopathies v0.20 SUFU Zornitza Stark Gene: sufu has been classified as Amber List (Moderate Evidence).
Joubert syndrome and other neurological ciliopathies v0.20 SUFU Zornitza Stark Phenotypes for gene: SUFU were changed from to Joubert syndrome 32, MIM#617757
Joubert syndrome and other neurological ciliopathies v0.19 SUFU Zornitza Stark Publications for gene: SUFU were set to
Joubert syndrome and other neurological ciliopathies v0.18 SUFU Zornitza Stark Mode of inheritance for gene: SUFU was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Joubert syndrome and other neurological ciliopathies v0.17 SUFU Zornitza Stark Classified gene: SUFU as Amber List (moderate evidence)
Joubert syndrome and other neurological ciliopathies v0.17 SUFU Zornitza Stark Gene: sufu has been classified as Amber List (Moderate Evidence).
Joubert syndrome and other neurological ciliopathies v0.16 SUFU Zornitza Stark reviewed gene: SUFU: Rating: AMBER; Mode of pathogenicity: None; Publications: 28965847; Phenotypes: Joubert syndrome 32, MIM#617757; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2267 SUFU Zornitza Stark Marked gene: SUFU as ready
Intellectual disability syndromic and non-syndromic v0.2267 SUFU Zornitza Stark Gene: sufu has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2267 SUFU Zornitza Stark Classified gene: SUFU as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.2267 SUFU Zornitza Stark Gene: sufu has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.2266 SUFU Zornitza Stark gene: SUFU was added
gene: SUFU was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: SUFU was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SUFU were set to 28965847
Phenotypes for gene: SUFU were set to Joubert syndrome 32, MIM#617757
Review for gene: SUFU was set to AMBER
Added comment: Two unrelated families described with what are postulated to be hypomorphic bi-allelic variants in this gene and Joubert syndrome. Note gene also causes dominant Basal Cell Nevus Syndrome.
Sources: Expert list
Intellectual disability syndromic and non-syndromic v0.2265 STX11 Zornitza Stark Marked gene: STX11 as ready
Intellectual disability syndromic and non-syndromic v0.2265 STX11 Zornitza Stark Gene: stx11 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2265 STX11 Zornitza Stark Phenotypes for gene: STX11 were changed from to Hemophagocytic lymphohistiocytosis, familial, 4, MIM# 603552
Intellectual disability syndromic and non-syndromic v0.2264 STX11 Zornitza Stark Mode of inheritance for gene: STX11 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2263 STX11 Zornitza Stark Classified gene: STX11 as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2263 STX11 Zornitza Stark Gene: stx11 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2262 STX11 Zornitza Stark reviewed gene: STX11: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hemophagocytic lymphohistiocytosis, familial, 4, MIM# 603552; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2262 STT3A Zornitza Stark edited their review of gene: STT3A: Changed rating: GREEN; Changed publications: 23842455, 30701557, 28424003; Changed phenotypes: Congenital disorder of glycosylation, type Iw, OMIM #615596; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2262 STRADA Zornitza Stark Marked gene: STRADA as ready
Intellectual disability syndromic and non-syndromic v0.2262 STRADA Zornitza Stark Gene: strada has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2262 STRADA Zornitza Stark Classified gene: STRADA as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.2262 STRADA Zornitza Stark Gene: strada has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.2261 STRADA Zornitza Stark gene: STRADA was added
gene: STRADA was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list
Mode of inheritance for gene: STRADA was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: STRADA were set to 17522105; 27170158; 28688840
Phenotypes for gene: STRADA were set to Polyhydramnios, megalencephaly, and symptomatic epilepsy, MIM# 611087
Review for gene: STRADA was set to GREEN
Added comment: Seven distantly related Menonite children plus four other unrelated families reported.
Sources: Expert list
Polymicrogyria and Schizencephaly v0.26 SRPX2 Zornitza Stark Marked gene: SRPX2 as ready
Polymicrogyria and Schizencephaly v0.26 SRPX2 Zornitza Stark Gene: srpx2 has been classified as Red List (Low Evidence).
Polymicrogyria and Schizencephaly v0.26 SRPX2 Zornitza Stark Phenotypes for gene: SRPX2 were changed from to Rolandic epilepsy, mental retardation, and speech dyspraxia, MIM# 300643
Polymicrogyria and Schizencephaly v0.25 SRPX2 Zornitza Stark Publications for gene: SRPX2 were set to
Polymicrogyria and Schizencephaly v0.24 SRPX2 Zornitza Stark Mode of inheritance for gene: SRPX2 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Polymicrogyria and Schizencephaly v0.23 SRPX2 Zornitza Stark Classified gene: SRPX2 as Red List (low evidence)
Polymicrogyria and Schizencephaly v0.23 SRPX2 Zornitza Stark Gene: srpx2 has been classified as Red List (Low Evidence).
Polymicrogyria and Schizencephaly v0.22 SRPX2 Zornitza Stark reviewed gene: SRPX2: Rating: RED; Mode of pathogenicity: None; Publications: 16497722, 23933820, 23871722; Phenotypes: Rolandic epilepsy, mental retardation, and speech dyspraxia, MIM# 300643; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Mendeliome v0.1521 SRPX2 Zornitza Stark Marked gene: SRPX2 as ready
Mendeliome v0.1521 SRPX2 Zornitza Stark Gene: srpx2 has been classified as Red List (Low Evidence).
Mendeliome v0.1521 SRPX2 Zornitza Stark Phenotypes for gene: SRPX2 were changed from to Rolandic epilepsy, mental retardation, and speech dyspraxia, MIM# 300643
Mendeliome v0.1520 SRPX2 Zornitza Stark Publications for gene: SRPX2 were set to
Mendeliome v0.1519 SRPX2 Zornitza Stark Mode of inheritance for gene: SRPX2 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Mendeliome v0.1518 SRPX2 Zornitza Stark Classified gene: SRPX2 as Red List (low evidence)
Mendeliome v0.1518 SRPX2 Zornitza Stark Gene: srpx2 has been classified as Red List (Low Evidence).
Mendeliome v0.1517 SRPX2 Zornitza Stark reviewed gene: SRPX2: Rating: RED; Mode of pathogenicity: None; Publications: 16497722, 23933820, 23871722; Phenotypes: Rolandic epilepsy, mental retardation, and speech dyspraxia, MIM# 300643; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Intellectual disability syndromic and non-syndromic v0.2260 SRPX2 Zornitza Stark Marked gene: SRPX2 as ready
Intellectual disability syndromic and non-syndromic v0.2260 SRPX2 Zornitza Stark Gene: srpx2 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2260 SRPX2 Zornitza Stark Phenotypes for gene: SRPX2 were changed from to Rolandic epilepsy, mental retardation, and speech dyspraxia, MIM# 300643
Intellectual disability syndromic and non-syndromic v0.2259 SRPX2 Zornitza Stark Publications for gene: SRPX2 were set to
Intellectual disability syndromic and non-syndromic v0.2258 SRPX2 Zornitza Stark Mode of inheritance for gene: SRPX2 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Intellectual disability syndromic and non-syndromic v0.2257 SRPX2 Zornitza Stark Classified gene: SRPX2 as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2257 SRPX2 Zornitza Stark Gene: srpx2 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2256 SRPX2 Zornitza Stark reviewed gene: SRPX2: Rating: RED; Mode of pathogenicity: None; Publications: 16497722, 23933820, 23871722; Phenotypes: Rolandic epilepsy, mental retardation, and speech dyspraxia, MIM# 300643; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Bone Marrow Failure v0.28 SRP54 Zornitza Stark Marked gene: SRP54 as ready
Bone Marrow Failure v0.28 SRP54 Zornitza Stark Gene: srp54 has been classified as Green List (High Evidence).
Bone Marrow Failure v0.28 SRP54 Zornitza Stark Phenotypes for gene: SRP54 were changed from to Syndromic neutropenia with Shwachman-Diamond-like features
Bone Marrow Failure v0.27 SRP54 Zornitza Stark Publications for gene: SRP54 were set to
Bone Marrow Failure v0.26 SRP54 Zornitza Stark Mode of inheritance for gene: SRP54 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Bone Marrow Failure v0.25 SRP54 Zornitza Stark reviewed gene: SRP54: Rating: GREEN; Mode of pathogenicity: None; Publications: 28972538; Phenotypes: Syndromic neutropenia with Shwachman-Diamond-like features; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1517 SPRTN Zornitza Stark Marked gene: SPRTN as ready
Mendeliome v0.1517 SPRTN Zornitza Stark Gene: sprtn has been classified as Green List (High Evidence).
Mendeliome v0.1517 SPRTN Zornitza Stark Phenotypes for gene: SPRTN were changed from to Ruijs-Aalfs syndrome, MIM# 616200
Mendeliome v0.1516 SPRTN Zornitza Stark Publications for gene: SPRTN were set to
Mendeliome v0.1515 SPRTN Zornitza Stark Mode of inheritance for gene: SPRTN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1514 SPRTN Zornitza Stark reviewed gene: SPRTN: Rating: GREEN; Mode of pathogenicity: None; Publications: 25261934; Phenotypes: Ruijs-Aalfs syndrome, MIM# 616200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2256 SPRTN Zornitza Stark Marked gene: SPRTN as ready
Intellectual disability syndromic and non-syndromic v0.2256 SPRTN Zornitza Stark Gene: sprtn has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2256 SPRTN Zornitza Stark Phenotypes for gene: SPRTN were changed from to Ruijs-Aalfs syndrome, MIM# 616200
Intellectual disability syndromic and non-syndromic v0.2255 SPRTN Zornitza Stark Publications for gene: SPRTN were set to
Intellectual disability syndromic and non-syndromic v0.2254 SPRTN Zornitza Stark Mode of inheritance for gene: SPRTN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.2253 SPRTN Zornitza Stark Classified gene: SPRTN as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.2253 SPRTN Zornitza Stark Gene: sprtn has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.2252 SPRTN Zornitza Stark reviewed gene: SPRTN: Rating: RED; Mode of pathogenicity: None; Publications: 25261934; Phenotypes: Ruijs-Aalfs syndrome, MIM# 616200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Long QT Syndrome v0.5 SCN5A Zornitza Stark Marked gene: SCN5A as ready
Long QT Syndrome v0.5 SCN5A Zornitza Stark Gene: scn5a has been classified as Green List (High Evidence).
Long QT Syndrome v0.5 SCN5A Zornitza Stark Phenotypes for gene: SCN5A were changed from to Long QT syndrome 3 (MIM#603830)
Long QT Syndrome v0.5 SCN5A Zornitza Stark Publications for gene: SCN5A were set to 29798782
Long QT Syndrome v0.4 SCN5A Zornitza Stark Publications for gene: SCN5A were set to
Long QT Syndrome v0.4 SCN5A Zornitza Stark Mode of inheritance for gene: SCN5A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1514 MC4R Zornitza Stark Marked gene: MC4R as ready
Mendeliome v0.1514 MC4R Zornitza Stark Gene: mc4r has been classified as Green List (High Evidence).