Left Ventricular Noncompaction Cardiomyopathy
Gene: DNAJC19EnsemblGeneIds (GRCh38): ENSG00000205981
EnsemblGeneIds (GRCh37): ENSG00000205981
OMIM: 608977, Gene2Phenotype
DNAJC19 is in 15 panels
1 review
Oxford Medical Genetics Laboratory (OUH NHS Foundation Trust)
Details
- Sources
-
- Expert Review Red
- Expert list
- OMIM
- 608977
- Clinvar variants
- Variants in DNAJC19
- Penetrance
- Complete
- Panels with this gene
-
- Possible mitochondrial disorder, nuclear genes
- Mitochondrial disorders
- Fetal anomalies
- Neurodegenerative disorders, adult onset
- Hereditary ataxia, adult onset
- Left Ventricular Noncompaction Cardiomyopathy
- Ataxia and cerebellar anomalies - childhood onset
- Paediatric or syndromic cardiomyopathy
- Likely inborn error of metabolism
- Undiagnosed metabolic disorders
- Dilated Cardiomyopathy and conduction defects
- Optic neuropathy
- Hereditary ataxia
- Intellectual disability
- Dystonia, chorea or related movement disorder, childhood onset
History Filter Activity
Gene classified by Genomics England curator
Caroline Wright (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Added New Source
Ellen McDonagh (Genomics England Curator)DNAJC19 was added to Left ventricular non-compaction cardiomyopathypanel. Sources: Expert list