GLA Chromosome X

Galactosidase alpha
547 variants 547 Health Risk

Upload your DNA to see your personal genotypes for variants in GLA.

What This Gene Does
This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Galactosidases alpha
Locus Type
gene with protein product
Location
Xq22.1
Ensembl
ENSG00000102393
Associated Conditions (14)
Fabry disease
Cardiovascular phenotype
GLA-related disorder
Cardiomyopathy
Migalastat response
Charcot-Marie-Tooth disease
Primary familial hypertrophic cardiomyopathy
Nonpapillary renal cell carcinoma
cardiac variant
Hypertrophic cardiomyopathy
Nephrotic syndrome
Thyroid cancer
nonmedullary
1
Key Variants
All Variants (547)
RSID Category Clinical Significance Conditions
RS730880442 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease, Fabry disease
RS730880450 Health Risk Pathogenic/Likely pathogenic Fabry disease, Cardiovascular phenotype, GLA-related disorder
RS730880451 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS730880454 Health Risk Pathogenic/Likely pathogenic Fabry disease, Cardiovascular phenotype, Fabry disease
RS730880455 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS782197638 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS782509013 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS797044499 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease, Cardiovascular phenotype
RS797044500 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS797044727 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease, Fabry disease
RS797044746 Health Risk Pathogenic/Likely pathogenic Cardiovascular phenotype, Fabry disease, Cardiovascular phenotype
RS797044748 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS797044749 Health Risk Pathogenic/Likely pathogenic Fabry disease, Cardiovascular phenotype, Fabry disease
RS797044775 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS797044776 Health Risk Pathogenic/Likely pathogenic Fabry disease, Cardiovascular phenotype, Fabry disease
RS797044777 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS868923658 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease, Thyroid cancer
RS869312134 Health Risk Pathogenic/Likely pathogenic Migalastat response, Fabry disease, Migalastat response
RS869312135 Health Risk Pathogenic/Likely pathogenic Fabry disease, Migalastat response, Fabry disease
RS869312142 Health Risk Pathogenic/Likely pathogenic Fabry disease, Migalastat response, Fabry disease
RS869312148 Health Risk Pathogenic/Likely pathogenic Fabry disease, Migalastat response, Fabry disease
RS869312226 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease, Fabry disease
RS869312230 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS869312233 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS869312241 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS869312246 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS869312255 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease, Fabry disease
RS869312272 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS869312310 Health Risk Pathogenic/Likely pathogenic Fabry disease, Cardiovascular phenotype, Fabry disease
RS869312311 Health Risk Pathogenic/Likely pathogenic Fabry disease, Cardiomyopathy, Fabry disease
RS869312324 Health Risk Pathogenic/Likely pathogenic Fabry disease, Cardiovascular phenotype, Fabry disease
RS869312342 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease, Fabry disease
RS869312381 Health Risk Pathogenic/Likely pathogenic Fabry disease, Cardiovascular phenotype, Hypertrophic cardiomyopathy
RS869312382 Health Risk Pathogenic/Likely pathogenic Fabry disease, Cardiovascular phenotype, Fabry disease
RS869312396 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS869312399 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease, Cardiovascular phenotype
RS869312400 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease, GLA-related disorder
RS869312404 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS869312406 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS869312408 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease, Fabry disease
RS869312440 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS869312441 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS869312448 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS886039136 Health Risk Pathogenic/Likely pathogenic Cardiovascular phenotype, Fabry disease, Cardiomyopathy
RS886044829 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS886044843 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
RS886044879 Health Risk Pathogenic/Likely pathogenic Fabry disease, Fabry disease
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