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
-
- Undiagnosed metabolic disorders
- Left Ventricular Noncompaction Cardiomyopathy
- Dilated Cardiomyopathy and conduction defects
- Optic neuropathy
- Likely inborn error of metabolism
- Paediatric or syndromic cardiomyopathy
- Ataxia and cerebellar anomalies - narrow panel
- Adult onset neurodegenerative disorder
- Mitochondrial disorders
- Intellectual disability
- Hereditary ataxia with onset in adulthood
- Childhood onset dystonia, chorea or related movement disorder
- Hereditary ataxia
- Possible mitochondrial disorder - nuclear genes
- Fetal anomalies
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