Proteinuria
Gene: COQ8AEnsemblGeneIds (GRCh38): ENSG00000163050
EnsemblGeneIds (GRCh37): ENSG00000163050
OMIM: 606980, Gene2Phenotype
COQ8A is in 13 panels
2 reviews
Ain Roesley (Victorian Clinical Genetics Services)
PMID 32337771: cohort of 59 individuals. COQ8A-ataxia presented as variable multisystemic, early-onset cerebellar ataxia, with complicating features ranging from epilepsy (32%) and cognitive impairment (49%) to exercise intolerance (25%) and hyperkinetic movement disorders (41%), including dystonia and myoclonus as presenting symptoms.Created: 4 May 2022, 2:47 a.m. | Last Modified: 4 May 2022, 2:47 a.m.
Panel Version: 0.13679
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Coenzyme Q10 deficiency, primary, 4 MIM#612016
Publications
Variants in this GENE are reported as part of current diagnostic practice
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
SRNS described in COQ8B related disease not COQ8A.Created: 20 Dec 2019, 1:52 a.m. | Last Modified: 20 Dec 2019, 1:52 a.m.
Panel Version: 0.17
Phenotypes
Coenzyme Q10 deficiency, primary, 4, MIM#612016
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Green
- Expert Review Red
- Victorian Clinical Genetics Services
- Phenotypes
-
- Coenzyme Q10 deficiency, primary, 4, MIM#612016
- OMIM
- 606980
- Clinvar variants
- Variants in COQ8A
- Penetrance
- None
- Panels with this gene
-
- Rhabdomyolysis and Metabolic Myopathy
- Regression
- Mackenzie's Mission_Reproductive Carrier Screening
- Leukodystrophy - paediatric
- Prepair 1000+
- Dystonia - complex
- Proteinuria
- Mendeliome
- BabyScreen+ newborn screening
- Mitochondrial disease
- Intellectual disability syndromic and non-syndromic
- Ataxia - paediatric
- Genetic Epilepsy
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: coq8a has been classified as Red List (Low Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: COQ8A were changed from to Coenzyme Q10 deficiency, primary, 4, MIM#612016
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: coq8a has been classified as Red List (Low Evidence).
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: COQ8A was added gene: COQ8A was added to Nephrotic Syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: COQ8A was set to Unknown