Gene Gene information from NCBI Gene database.
Entrez ID 2717
Gene name Galactosidase alpha
Gene symbol GLA
Synonyms (NCBI Gene)
GALA
Chromosome X
Chromosome location Xq22.1
Summary 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 galacto
miRNA miRNA information provided by mirtarbase database.
28
miRTarBase ID miRNA Experiments Reference
MIRT039851 hsa-miR-615-3p CLASH 23622248
MIRT039206 hsa-miR-769-5p CLASH 23622248
MIRT519448 hsa-miR-6758-5p PAR-CLIP 23446348
MIRT519447 hsa-miR-6856-5p PAR-CLIP 23446348
MIRT519445 hsa-miR-6732-5p PAR-CLIP 23446348
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
38
GO ID Ontology Definition Evidence Reference
GO:0003824 Function Catalytic activity IDA 39940
GO:0004553 Function Hydrolase activity, hydrolyzing O-glycosyl compounds IEA
GO:0004557 Function Alpha-galactosidase activity IBA
GO:0004557 Function Alpha-galactosidase activity IDA 39940, 8804427, 27211852
GO:0004557 Function Alpha-galactosidase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300644 4296 ENSG00000102393
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P06280
Protein name Alpha-galactosidase A (EC 3.2.1.22) (Alpha-D-galactosidase A) (Alpha-D-galactoside galactohydrolase) (Galactosylgalactosylglucosylceramidase GLA) (Melibiase) (Agalsidase)
Protein function Catalyzes the hydrolysis of glycosphingolipids and participates in their degradation in the lysosome.
PDB 1R46 , 1R47 , 3GXN , 3GXP , 3GXT , 3HG2 , 3HG3 , 3HG4 , 3HG5 , 3LX9 , 3LXA , 3LXB , 3LXC , 3S5Y , 3S5Z , 3TV8 , 4NXS , 6IBK , 6IBM , 6IBR , 6IBT , 8K7D , 8K7E , 8K7F , 8K7G , 8K7H , 8K7I , 8K7J , 8K7K , 8K7L , 9AVS
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF16499 Melibiase_2 39 322 Alpha galactosidase A Family
PF17450 Melibiase_2_C 325 411 Alpha galactosidase A C-terminal beta sandwich domain Domain
Sequence
Sequence length 429
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Galactose metabolism
Glycerolipid metabolism
Sphingolipid metabolism
Glycosphingolipid biosynthesis - globo and isoglobo series
Metabolic pathways
Lysosome
  Glycosphingolipid metabolism
Neutrophil degranulation
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
20
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Cardiomyopathy Likely pathogenic; Pathogenic rs869312311, rs28935197, rs199473684, rs397515870, rs886039136 RCV001799418
RCV001798000
RCV000769537
RCV000769540
RCV000769542
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Cardiovascular phenotype Likely pathogenic; Pathogenic rs1928323615, rs2147487910, rs2147487830, rs869312429, rs727503949, rs398123224, rs1183869568, rs730880441, rs730880440, rs730880450, rs730880454, rs2520895216, rs869312310, rs2520849107, rs2520852645
View all (33 more)
RCV006347710
RCV004629626
RCV003303377
RCV002423245
RCV005572276
View all (43 more)
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Fabry disease Likely pathogenic; Pathogenic rs1928194190, rs398123208, rs1928323615, rs2147471863, rs869312408, rs2147472050, rs28935485, rs869312305, rs2147480697, rs2147487910, rs2147472959, rs2147470514, rs2147477659, rs2147477845, rs387906483
View all (424 more)
RCV001321823
RCV001328356
RCV001341700
RCV001358705
RCV001358704
View all (512 more)
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Fabry disease, cardiac variant Likely pathogenic; Pathogenic rs869312142, rs104894828, rs104894830, rs28935485, rs104894846, rs104894847, rs199473684, rs886044878 RCV001636724
RCV000011461
RCV000011464
RCV000011468
RCV000011510
View all (3 more)
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ANGIOKERATOMA CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIOMYOPATHIES Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1 Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIOMYOPATHY, HYPERTROPHIC, FAMILIAL Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations