GLA Chromosome X

Galactosidase alpha
547 variants 547 Health Risk

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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
RS2520897726 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS2520914744 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS28935487 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease, Fabry disease
RS28935488 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease, Migalastat response
RS28935490 Health Risk Conflicting classifications of pathogenicity Migalastat response, Fabry disease, Cardiovascular phenotype
RS372416832 Health Risk Conflicting classifications of pathogenicity Fabry disease, Cardiovascular phenotype, GLA-related disorder
RS375538532 Health Risk Conflicting classifications of pathogenicity Fabry disease, Cardiovascular phenotype, Fabry disease
RS375661583 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS397515868 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS397515870 Health Risk Conflicting classifications of pathogenicity Fabry disease, Cardiomyopathy, Cardiovascular phenotype
RS397515872 Health Risk Conflicting classifications of pathogenicity Fabry disease, Cardiovascular phenotype, Cardiomyopathy
RS397515873 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS397515874 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS398123200 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS398123204 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS398123209 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS398123213 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS398123227 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS727503948 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease, Fabry disease
RS727503950 Health Risk Conflicting classifications of pathogenicity Fabry disease, Migalastat response, Cardiovascular phenotype
RS727503951 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS727504689 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS727505060 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS730880437 Health Risk Conflicting classifications of pathogenicity Fabry disease, Cardiovascular phenotype, Fabry disease
RS730880438 Health Risk Conflicting classifications of pathogenicity Fabry disease, Cardiovascular phenotype, Fabry disease
RS781838005 Health Risk Conflicting classifications of pathogenicity Fabry disease, Migalastat response, Cardiovascular phenotype
RS781871113 Health Risk Conflicting classifications of pathogenicity Fabry disease, Cardiovascular phenotype, Fabry disease
RS781906252 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS782051708 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS782164084 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS782200316 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS782362194 Health Risk Conflicting classifications of pathogenicity Fabry disease, Cardiovascular phenotype, Fabry disease
RS782442966 Health Risk Conflicting classifications of pathogenicity Fabry disease, Cardiovascular phenotype, Fabry disease
RS782506652 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS782561648 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS782690996 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS782722577 Health Risk Conflicting classifications of pathogenicity Fabry disease, Cardiovascular phenotype, Charcot-Marie-Tooth disease
RS782722844 Health Risk Conflicting classifications of pathogenicity Fabry disease, Cardiovascular phenotype, GLA-related disorder
RS869312145 Health Risk Conflicting classifications of pathogenicity Fabry disease, Migalastat response, Cardiovascular phenotype
RS869312163 Health Risk Conflicting classifications of pathogenicity Fabry disease, Migalastat response, Fabry disease
RS869312249 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS869312274 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS869312345 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS869312407 Health Risk Conflicting classifications of pathogenicity Fabry disease, Cardiovascular phenotype, Fabry disease
RS869312437 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS869312438 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease, Fabry disease
RS886044767 Health Risk Conflicting classifications of pathogenicity Fabry disease, Fabry disease
RS886044779 Health Risk Conflicting classifications of pathogenicity Fabry disease, Cardiovascular phenotype, Fabry disease
RS104894843 Health Risk Likely pathogenic Fabry disease, GLA-related disorder, Fabry disease
RS104894848 Health Risk Likely pathogenic Fabry disease, Fabry disease
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