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
-
- Left Ventricular Noncompaction Cardiomyopathy
- Neurodegenerative disorders, adult onset
- Paediatric or syndromic cardiomyopathy
- Undiagnosed metabolic disorders
- Dilated Cardiomyopathy and conduction defects
- Hereditary ataxia
- Optic neuropathy
- Intellectual disability
- Fetal anomalies
- Dystonia, chorea or related movement disorder, childhood onset
- Ataxia and cerebellar anomalies - childhood onset
- Hereditary ataxia, adult onset
- Possible mitochondrial disorder, nuclear genes
- Mitochondrial disorders
- Likely inborn error of metabolism
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