Dilated Cardiomyopathy (DCM)
Gene: GLAEnsemblGeneIds (GRCh38): ENSG00000102393
EnsemblGeneIds (GRCh37): ENSG00000102393
OMIM: 300644, Gene2Phenotype
GLA is in 25 panels
1 review
Oxford Medical Genetics Laboratory (OUH NHS Foundation Trust)
Variants in this GENE are reported as part of current diagnostic practice
Details
- Sources
-
- OMIM
- 300644
- Clinvar variants
- Variants in GLA
- Penetrance
- Complete
- Panels with this gene
-
- Cystic kidney disease
- Proteinuric renal disease
- Lysosomal storage disorder
- Likely inborn error of metabolism
- Paediatric or syndromic cardiomyopathy
- Neurodegenerative disorders, adult onset
- Cerebral vascular malformations
- Undiagnosed metabolic disorders
- Leukodystrophy, adult onset
- Dilated Cardiomyopathy and conduction defects
- Mucopolysaccharideosis, Gaucher, Fabry
- Hyperammonaemia
- Dystonia, chorea or related movement disorder, childhood onset
- Hereditary neuropathy or pain disorder
- Fetal hydrops
- Hypertrophic cardiomyopathy
- Paroxysmal central nervous system disorders
- Progressive cardiac conduction disease
- Unexplained kidney failure in young people
- Hereditary neuropathy
- Fetal anomalies
- Pain syndromes
- Fabry disease
- Multiple monogenic benign skin tumours
- Familial cerebral small vessel disease
History Filter Activity
Approved Gene
Caroline Wright (Genomics England Curator)This proposed gene was validated and added to this panel
Created
Oxford Medical Genetics Laboratory (OUH NHS Foundation Trust)GLA was created by OxfordGenetics
Added New Source
Oxford Medical Genetics Laboratory (OUH NHS Foundation Trust)GLA was added to Dilated Cardiomyopathy (DCM)panel. Sources: Oxford Medical Genetics Laboratory