This Panel is marked as Deleted
Kidneyome_SuperPanel_KidGen_VCGS
Gene: COQ8A
COQ8A (coenzyme Q8A)
EnsemblGeneIds (GRCh38): ENSG00000163050
EnsemblGeneIds (GRCh37): ENSG00000163050
OMIM: 606980, Gene2Phenotype
COQ8A is in 18 panels
EnsemblGeneIds (GRCh38): ENSG00000163050
EnsemblGeneIds (GRCh37): ENSG00000163050
OMIM: 606980, Gene2Phenotype
COQ8A is in 18 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Red
- Phenotypes
-
- Coenzyme Q10 deficiency, primary, 4, MIM#612016
- OMIM
- 606980
- Clinvar variants
- Variants in COQ8A
- Penetrance
- None
- Panels with this gene
-
- Hereditary neuropathy or pain disorder
- Likely inborn error of metabolism
- Acute rhabdomyolysis
- Undiagnosed metabolic disorders
- Inherited white matter disorders
- Hereditary ataxia
- Ataxia and cerebellar anomalies - narrow panel
- Hereditary ataxia with onset in adulthood
- Intellectual disability
- Adult onset neurodegenerative disorder
- Childhood onset dystonia, chorea or related movement disorder
- Mitochondrial disorders
- Rhabdomyolysis and metabolic muscle disorders
- DDG2P
- White matter disorders and cerebral calcification - narrow panel
- Possible mitochondrial disorder - nuclear genes
- Hereditary neuropathy
- Fetal anomalies
History Filter Activity
24 Dec 2019, Gel status: 1
Set Phenotypes
Ivone Leong (Genomics England Curator)Added phenotypes Coenzyme Q10 deficiency, primary, 4, MIM#612016 for gene: COQ8A
23 Dec 2019, Gel status: 1
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Ivone Leong (Genomics England Curator)gene: COQ8A was added gene: COQ8A was added to Kidneyome_SuperPanel_KidGen_VCGS. Sources: Expert Review Red,Victorian Clinical Genetics Services Mode of inheritance for gene: COQ8A was set to Unknown Phenotypes for gene: COQ8A were set to Coenzyme Q10 deficiency, primary, 4, MIM#612016