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