This Panel is marked as Retired
Dilated Cardiomyopathy (DCM)
Gene: GLA
GLA (galactosidase alpha)
EnsemblGeneIds (GRCh38): ENSG00000102393
EnsemblGeneIds (GRCh37): ENSG00000102393
OMIM: 300644, Gene2Phenotype
GLA is in 25 panels
EnsemblGeneIds (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
-
- Hereditary neuropathy
- Lysosomal storage disorder
- Fabry disease
- Paediatric or syndromic cardiomyopathy
- Hereditary neuropathy or pain disorder
- Multiple monogenic benign skin tumours
- Likely inborn error of metabolism
- Undiagnosed metabolic disorders
- Dilated Cardiomyopathy and conduction defects
- Cystic kidney disease
- Progressive cardiac conduction disease
- Mucopolysaccharideosis, Gaucher, Fabry
- Hyperammonaemia
- Fetal hydrops
- Fetal anomalies
- Cerebral vascular malformations
- Adult onset leukodystrophy
- Paroxysmal central nervous system disorders
- Adult onset neurodegenerative disorder
- Childhood onset dystonia, chorea or related movement disorder
- Unexplained kidney failure in young people
- Proteinuric renal disease
- Pain syndromes
- Hypertrophic cardiomyopathy
- Familial cerebral small vessel disease
History Filter Activity
11 Feb 2016, Gel status: 0
Approved Gene
Caroline Wright (Genomics England Curator)This proposed gene was validated and added to this panel
6 Jan 2016, Gel status: 0
Created
Oxford Medical Genetics Laboratory (OUH NHS Foundation Trust)GLA was created by OxfordGenetics
6 Jan 2016, Gel status: 0
Added New Source
Oxford Medical Genetics Laboratory (OUH NHS Foundation Trust)GLA was added to Dilated Cardiomyopathy (DCM)panel. Sources: Oxford Medical Genetics Laboratory