This Panel is marked as Deleted
Mitochondrial disorders Victorian Clinical Genetics Services
Gene: DNAJC19
DNAJC19 (DnaJ heat shock protein family (Hsp40) member C19)
EnsemblGeneIds (GRCh38): ENSG00000205981
EnsemblGeneIds (GRCh37): ENSG00000205981
OMIM: 608977, Gene2Phenotype
DNAJC19 is in 15 panels
EnsemblGeneIds (GRCh38): ENSG00000205981
EnsemblGeneIds (GRCh37): ENSG00000205981
OMIM: 608977, Gene2Phenotype
DNAJC19 is in 15 panels
0 reviews
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 608977
- Clinvar variants
- Variants in DNAJC19
- Penetrance
- None
- Panels with this gene
-
- Adult onset neurodegenerative disorder
- Left Ventricular Noncompaction Cardiomyopathy
- Undiagnosed metabolic disorders
- Intellectual disability
- Dilated Cardiomyopathy and conduction defects
- Childhood onset dystonia, chorea or related movement disorder
- Optic neuropathy
- Paediatric or syndromic cardiomyopathy
- Fetal anomalies
- Mitochondrial disorders
- Hereditary ataxia with onset in adulthood
- Hereditary ataxia
- Possible mitochondrial disorder - nuclear genes
- Likely inborn error of metabolism
- Ataxia and cerebellar anomalies - narrow panel
History Filter Activity
12 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)DNAJC19 was added to Mitochondrial disorders Victorian Clinical Genetics Services panel. Sources: Expert Review Green,Victorian Clinical Genetics Services
12 Jun 2018, Gel status: 4
Created
Sarah Leigh (Genomics England Curator)DNAJC19 was created by Sarah Leigh