1. Panels
  2. Monogenic Diabetes

Monogenic Diabetes (Version 0.136)

Level 2: Endocrine disorders

Relevant disorders: Diabetes mellitus, HP:0000819
Panel types: Victorian Clinical Genetics Services, Royal Melbourne Hospital, Rare Disease
Description
This panel was created by consolidating the following Genomics England PanelApp panels: Monogenic Diabetes, Multi-organ autoimmune diabetes, Diabetes with additional phenotypes suggestive of a monogenic aetiology, Familial Diabetes and Diabetes - neonatal onset. It is maintained by VCGS.
Panel Activity

9 reviewers

  • Teresa Zhao (Victorian Clinical Genetics Services)

  • Chirag Patel (Genetic Health Queensland)

  • Krithika Murali (Victorian Clinical Genetics Services)

  • Michelle Torres (Victorian Clinical Genetics Services)

  • Elena Savva (Victorian Clinical Genetics Services)

  • Bryony Thompson (Royal Melbourne Hospital)

  • Seb Lunke (Victorian Clinical Genetics Services)

  • Hali Van Niel (University of Melbourne)

  • Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

77 Entities

77 reviewed, 55 green

List Entity Reviews Mode of inheritance Details
77 Entitiess
Green List (high evidence)
ABCC8
1 review
1 green 		BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • permanent neonatal diabetes mellitus MONDO:0100164
  • transient neonatal diabetes mellitus MONDO:0020525
Tags
Green List (high evidence)
AGPAT2
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • congenital generalized lipodystrophy type 1 MONDO:0012071
Tags
Green List (high evidence)
ALMS1
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
Phenotypes
  • Alstrom syndrome MONDO:0008763
Tags
Green List (high evidence)
BSCL2
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • congenital generalized lipodystrophy type 2 MONDO:0010020
  • diabetes mellitus MONDO:0005015
Tags
Green List (high evidence)
CISD2
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Wolfram syndrome, MIM#2604928
Tags
Green List (high evidence)
COQ2
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • coenzyme Q10 deficiency, primary, 1 MONDO:0011829
Tags
Green List (high evidence)
DCAF17
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Woodhouse-Sakati syndrome MONDO:0009419
Tags
Green List (high evidence)
DNAJC3
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome MONDO:0014523
Tags
Green List (high evidence)
EIF2AK3
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • UKGTN
Phenotypes
  • Wolcott-Rallison syndrome MONDO:0009192
  • neonatal diabetes mellitus MONDO:0016391
Tags
Green List (high evidence)
EIF2B1
1 review
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • Neonatal diabetes mellitus, MONDO:0016391, EIF2B1-related
Tags
Green List (high evidence)
EIF2S3
1 review
1 green 		X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • microcephaly
  • MEHMO syndrome (X-linked NDM and microcephaly),300148
  • diabetes
  • epilepsy
  • hypogonadism
  • intellectual disability
  • hypogenitalism
  • central obesity
Tags
Green List (high evidence)
FOXP3
1 review
1 green 		X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • UKGTN
Phenotypes
  • immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome MONDO:0010580
Tags
Green List (high evidence)
GATA4
2 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • NHS GMS
  • UKGTN
Phenotypes
  • neonatal diabetes mellitus MONDO:0016391
Tags
Green List (high evidence)
GATA6
1 review
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • pancreatic hypoplasia-diabetes-congenital heart disease syndrome MONDO:0010802
Tags
Green List (high evidence)
GCK
1 review
1 green 		BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Diabetes mellitus, noninsulin-dependent, late onset, AD (MIM#125853)
  • Diabetes mellitus, permanent neonatal 1, AR (MIM#606176)
  • Hyperinsulinemic hypoglycemia, familial, 3, AD (MIM#602485)
  • MODY, type II, AD (MIM#125851)
Tags
Green List (high evidence)
GLIS3
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • UKGTN
Phenotypes
  • neonatal diabetes mellitus with congenital hypothyroidism MONDO:0012436
Tags
Green List (high evidence)
HAMP
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • Hemochromatosis, type 2B 613313
Tags
Green List (high evidence)
HFE
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • haemochromatosis type 1 MONDO:0021001
Tags
Green List (high evidence)
HFE2
1 review
 BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • Hemochromatosis, type 2A, 602390
Tags
  • new gene name
Green List (high evidence)
HNF1A
1 review
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3
  • Maturity-Onset Diabetes Of The Young
  • MODY, type III, 600496
  • Maturity-onset diabetes of the young (MODY)
  • MODY, type III, 600496{Diabetes mellitus, noninsulin-dependent, 2}, 125853{Diabetes mellitus, insulin-dependent}, 222100Hepatic adenoma, somatic, 142330Renal cell carcinoma, 144700Diabetes mellitus, insulin-dependent, 20, 612520
  • {Diabetes mellitus, noninsulin-dependent, 2}, 125853
  • Diabetes mellitus, insulin-dependent, 20, 612520
  • {Diabetes mellitus, insulin-dependent}, 222100
  • Maturity Onset Diabetes of the Young
  • MODY3
Tags
Green List (high evidence)
HNF1B
1 review
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • renal cysts and diabetes syndrome MONDO:0007669
Tags
  • SV/CNV
Green List (high evidence)
HNF4A
1 review
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Fanconi renotubular syndrome 4, with maturity-onset diabetes of the young 616026
  • Maturity-Onset Diabetes Of The Young, Type 1
  • MODY1, 125850
  • {Diabetes mellitus, noninsulin-dependent}, 125853
Tags
Green List (high evidence)
IER3IP1
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • UKGTN
Phenotypes
  • Microcephaly, epilepsy, and diabetes syndrome, MIM# 614231
  • Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome, MONDO:0013647
Tags
Green List (high evidence)
IL2RA
1 review
 BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Neoantal diabetes, congenital hypothyrodism (multiple autoimmune) Recessive
  • {Diabetes, mellitus, insulin-dependent, susceptibility to, 10}, 601942
  • insulin-dependent diabetes mellitus at 8-weeks
  • IPEX-like syndrome
  • neonatal diabetes
Tags
Green List (high evidence)
INS
1 review
1 green 		BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • diabetes mellitus, permanent neonatal 4 MONDO:0030089
  • maturity-onset diabetes of the young type 10 MONDO:0013240
Tags
Green List (high evidence)
INSR
1 review
1 green 		BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • insulin-resistance syndrome type A MONDO:0012520
  • Rabson-Mendenhall syndrome MONDO:0009874
  • Donohue syndrome MONDO:0009517
Tags
Green List (high evidence)
KCNJ11
1 review
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • permanent neonatal diabetes mellitus MONDO:0100164
Tags
Green List (high evidence)
LMNA
1 review
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules
  • Severe insulin resistance, partial lipodystrophy and diabetes
  • FPLD2
  • LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2
  • Lipodystrophy, familial partial, 2, 151660
Tags
Green List (high evidence)
LRBA
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • Immunodeficiency, common variable, 8, with autoimmunity
Tags
Green List (high evidence)
MNX1
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • UKGTN
Phenotypes
  • Permanent neonatal diabetes mellitus, MONDO:0100164, MNX1-related
Tags
Green List (high evidence)
NEUROD1
1 review
1 green 		BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • maturity-onset diabetes of the young type 6 MONDO:0011668
Tags
Green List (high evidence)
NEUROG3
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • UKGTN
Phenotypes
  • congenital malabsorptive diarrhea 4 MONDO:0012479
Tags
Green List (high evidence)
NKX2-2
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • UKGTN
Phenotypes
  • Syndromic neonatal diabetes, with severe developmental delay, hypotonia, cortical blindness, hearing impairment
Tags
Green List (high evidence)
ONECUT1
2 reviews
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Syndromic diabetes
  • Neonatal diabetes mellitus MONDO:0016391
Tags
Green List (high evidence)
PCBD1
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Hyperphenylalaninemia, BH4-deficient, D, 264070
  • Recessive neonatal hyperphenylalaninemia and later onset diabetes (puberty)
Tags
Green List (high evidence)
PDX1
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • maturity-onset diabetes of the young type 4 MONDO:0011667
Tags
Green List (high evidence)
PIK3R1
1 review
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • SHORT syndrome MONDO:0010026
  • Short stature, hyperextensibility of joints and/or inguinal hernia, ocular depression, Rieger anomaly, and teething delay (SHORT) syndrome, MIM#269880
Tags
Green List (high evidence)
POLD1
1 review
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • mandibular hypoplasia-deafness-progeroid syndrome MONDO:0014157
Tags
Green List (high evidence)
PPARG
2 reviews
1 red 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Insulin resistance, severe, digenic
  • FPLD3
  • Obesity, severe, 601665
  • {Diabetes, type 2}, 125853
  • Lipodystrophy, familial partial, type 3
  • Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension
  • Insulin resistance, severe, digenic 604367
  • [Obesity, resistance to]
  • Lipodystrophy, familial partial, type 3, 604367
  • Insulin resistance, severe, digenic, 604367
  • Lipodystrophy, familial partial, type 3 604367
  • LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3
  • Carotid intimal medial thickness 1, 609338
Tags
Green List (high evidence)
PTF1A
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Diabetes mellitus, permanent neonatal, with cerebellar agenesis, MIM#609069
Tags
Green List (high evidence)
RFX6
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Mitchell-Riley syndrome, 615710
  • Neonatal diabetes, intestinal atresia and hepatobiliary abnormalities
  • recessive syndromic diabetes and autosomal dominant MODY
Tags
Green List (high evidence)
SLC19A2
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • UKGTN
Phenotypes
  • thiamine-responsive megaloblastic anemia syndrome MONDO:0009575
Tags
Green List (high evidence)
SLC29A3
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Histiocytosis-lymphadenopathy plus syndrome, MIM#602782
Tags
Green List (high evidence)
SLC2A2
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi-Bickel syndrome, MIM# 227810
Tags
Green List (high evidence)
SLC40A1
1 review
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • Hemochromatosis, type 4, MIM# 606069
Tags
Green List (high evidence)
SMPD4
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies MIM#618622
Tags
Green List (high evidence)
STAT3
1 review
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • UKGTN
Phenotypes
  • STAT3-related early-onset multisystem autoimmune disease MONDO:0014414
Tags
Green List (high evidence)
TFR2
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • Hemochromatosis, type 3 604250
Tags
Green List (high evidence)
TRMT10A
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Microcephaly, short stature, and impaired glucose metabolism 1, 616033
Tags
Green List (high evidence)
WFS1
1 review
1 green 		BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Wolfram-like syndrome, autosomal dominant, 614296
  • Wolfram syndrome, 222300
  • Deafness, autosomal dominant 6/14/38, 600965
  • ?Cataract 41,116400
  • {Diabetes mellitus, noninsulin-dependent, association with}, 125853
  • Deafness,autosomal dominant 6/14/38, 600965
  • {Diabetes mellitus, noninsulin-dependent,association with}
  • diabetes insipidus or optic atrophy
Tags
Green List (high evidence)
YIPF5
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Microcephaly, epilepsy, and diabetes syndrome 2 , MIM#619278
Tags
Green List (high evidence)
ZBTB20
1 review
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Primrose syndrome MONDO:0009798
  • Primrose syndrome (tall stature, macrocephaly, intellectual disability, disturbed behaviour, unusual facial features, diabetes, deafness, progressive muscle wasting and ectopic calcifications)
  • Primrose syndrome, 259050
Tags
Green List (high evidence)
ZFP57
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Diabetes mellitus, transient neonatal, 1, MIM#601410
Tags
Green List (high evidence)
ZMPSTE24
1 review
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
Phenotypes
  • Mandibuloacral dysplasia with type B lipodystrophy, 608612
Tags
Green List (high evidence)
ZNF808
2 reviews
2 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Pancreatic agenesis 3, MIM# 620991
Tags
Amber List (moderate evidence)
CEL
2 reviews
1 red 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • Diabetes and pancreatic exocrine dysfunction
  • Maturity-onset diabetes of the young, type VIII, 609812
Tags
Amber List (moderate evidence)
DYRK1B
1 review
 MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • Metabolic syndrome (coronary artery disease, hypertension, central obesity and diabetes)
  • Abdominal obesity-metabolic syndrome 3, 615812
Tags
Amber List (moderate evidence)
EPHX1
1 review
 MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Hereditary lipodystrophy, MONDO:0020087, EPHX1-related
Tags
Amber List (moderate evidence)
FICD
1 review
 BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Monogenic diabetes, MONDO:0015967, FICD-related
Tags
Amber List (moderate evidence)
MANF
1 review
 BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Amber
Phenotypes
  • Diabetes, deafness, developmental delay, and short stature syndrome, MIM# 620651
Tags
Amber List (moderate evidence)
PDIA6
2 reviews
 BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Asphyxiating thoracic dystrophy (ATD) syndrome and infantile‐onset diabetes
Tags
Amber List (moderate evidence)
PLIN1
1 review
 MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • Lipodystrophy, familial partial, type 4, 613877
  • Severe insulin resistance, partial lipodystrophy and diabetes
Tags
  • disputed
Amber List (moderate evidence)
PPP1R15B
1 review
 BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • Autosomal recessive juvenile-onset diabetes with microcephaly, epilepsy and intellectual disability,616817
Tags
Amber List (moderate evidence)
STAT1
1 review
 MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review
  • Expert Review Amber
Phenotypes
  • autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome MONDO:0013599
Tags
Red List (low evidence)
AGPS
1 review
1 red 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
Phenotypes
  • Lipodystrophy, congenital generalized, type 1, 608594
Tags
Red List (low evidence)
AKT2
1 review
1 red 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • NHS GMS
Phenotypes
  • Diabetes mellitus, type II, 125853
Tags
Red List (low evidence)
APPL1
1 review
1 red 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • NHS GMS
  • Royal Melbourne Hospital
Phenotypes
  • {Maturity-onset diabetes of the young, type 14}, 616511
  • Diabetes
Tags
Red List (low evidence)
BLK
1 review
1 red 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • Royal Melbourne Hospital
Phenotypes
  • Maturity-onset diabetes of the young, type 11, 613375
  • Maturity Onset Diabetes of the Young
Tags
Red List (low evidence)
CAV1
2 reviews
1 red 		BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Red
Phenotypes
  • Lipodystrophy, congenital generalized, type 3, 612526
  • Partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome
Tags
Red List (low evidence)
CIDEC
1 review
1 red 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
Phenotypes
  • CIDEC-related familial partial lipodystrophy MONDO:0014098
Tags
Red List (low evidence)
COQ9
1 review
1 red 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • NHS GMS
Phenotypes
  • encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome MONDO:0013840
Tags
Red List (low evidence)
DMXL2
1 review
1 red 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Other
Phenotypes
  • Polyendocrine-polyneuropathy syndrome , MIM# 616113
Tags
Red List (low evidence)
FOXC2
1 review
 Unknown
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Lymphedema-distichiasis syndrome, 153400
  • Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus, 153400
Tags
Red List (low evidence)
KLF11
1 review
 MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review
  • Expert Review Red
  • Royal Melbourne Hospital
Phenotypes
  • Maturity-onset diabetes of the young, type VII, 610508
  • Maturity Onset Diabetes of the Young
Tags
Red List (low evidence)
LIPC
1 review
1 red 		Unknown
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • {Diabetes mellitus, noninsulin-dependent}, MIM#125853
Tags
Red List (low evidence)
PAX4
3 reviews
2 green 1 red 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
  • Royal Melbourne Hospital
Phenotypes
  • Maturity-onset diabetes of the young, type IX MIM#612225
Tags
  • refuted
Red List (low evidence)
PAX6
2 reviews
2 red 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • NHS GMS
Phenotypes
  • Monogenic diabetes, MONDO:0015967, PAX6-related
Tags

Downloads

Download lists

  • Whole panel
  • Green list (high evidence)
  • Green and Amber Genes
  • Amber Genes
  • Red list (low evidence)

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