HCSGD entry for GLA


1. General information

Official gene symbolGLA
Entrez ID2717
Gene full namegalactosidase, alpha
Other gene symbolsGALA
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0003824Catalytic activityIDAmolecular_function
GO:0004557Alpha-galactosidase activityIDA IMP TASmolecular_function
GO:0005102Receptor bindingIDAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005576Extracellular regionIDA IMPcellular_component
GO:0005737CytoplasmIMPcellular_component
GO:0005764LysosomeIMP TAScellular_component
GO:0005794Golgi apparatusIMPcellular_component
GO:0006665Sphingolipid metabolic processTASbiological_process
GO:0006687Glycosphingolipid metabolic processTASbiological_process
GO:0009311Oligosaccharide metabolic processIDAbiological_process
GO:0016139Glycoside catabolic processIBAbiological_process
GO:0016787Hydrolase activityTASmolecular_function
GO:0016936Galactoside bindingIEAmolecular_function
GO:0042803Protein homodimerization activityIDAmolecular_function
GO:0043202Lysosomal lumenTAScellular_component
GO:0044281Small molecule metabolic processTASbiological_process
GO:0045019Negative regulation of nitric oxide biosynthetic processISSbiological_process
GO:0046477Glycosylceramide catabolic processIBA ISSbiological_process
GO:0046479Glycosphingolipid catabolic processTASbiological_process
GO:0051001Negative regulation of nitric-oxide synthase activityISSbiological_process
GO:0052692Raffinose alpha-galactosidase activityIEAmolecular_function
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.00124992210.73119643630.09514566471.0000000000

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Up1.0748797447
GSE13712_SHEARDown-0.1476107032
GSE13712_STATICDown-0.1152904593
GSE19018Up0.2915405553
GSE19899_A1Up1.6963953866
GSE19899_A2Up1.1520503625
PubMed_21979375_A1Up1.6374443960
PubMed_21979375_A2Up1.3384317602
GSE35957Down-0.5623753973
GSE36640Up1.1765052253
GSE54402Up1.2088480313
GSE9593Up0.7196933385
GSE43922Up1.1571080214
GSE24585Down-0.7394005886
GSE37065Up0.5046908691
GSE28863_A1Down-0.4489618571
GSE28863_A2Up0.2795294444
GSE28863_A3Down-0.4848628670
GSE28863_A4Up0.1096283146
GSE48662Down-0.0674627706

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Compound

Target

Confidence score

Uniprot

CHEMBL1163562CHEMBL25249P06280
CHEMBL469844CHEMBL25249P06280
CHEMBL1163255CHEMBL25249P06280
CHEMBL469844CHEMBL25249P06280
CHEMBL110458CHEMBL25249P06280
CHEMBL87169CHEMBL25248P06280
CHEMBL1169500CHEMBL25248P06280
CHEMBL358442CHEMBL25248P06280
CHEMBL307429CHEMBL25248P06280
CHEMBL13922CHEMBL25248P06280
CHEMBL110458CHEMBL25245P06280
CHEMBL176021CHEMBL25245P06280
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  • Drugs

Name

Drug

Accession number

MigalastatDB05018 -

  • MicroRNAs

  • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-769-5pMIMAT0003886MIRT039206CLASHFunctional MTI (Weak)23622248
hsa-miR-615-3pMIMAT0003283MIRT039851CLASHFunctional MTI (Weak)23622248
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  • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 3 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

16706651Among the most prevalent of these conditions are Gaucher disease and Fabry disease, which are caused by reduced activity of the housekeeping enzymes glucocerebrosidase and alpha-galactosidase A, respectively
11855860Four lysosomal enzyme activities were measured: beta-galactosidase, alpha-galactosidase A, beta-glucoronidase, and acid phosphatase
11855860TNF-alpha was the only agent that induced lysosomal activity in senescent fibroblasts, of which only alpha-galactosidase A activity was induced
8755577Correction in trans for Fabry disease: expression, secretion and uptake of alpha-galactosidase A in patient-derived cells driven by a high-titer recombinant retroviral vector
8755577Fabry disease is an X-linked metabolic disorder due to a deficiency of alpha-galactosidase A (alpha-gal A; EC 3
8755577Virus-producer cells also demonstrate expression of large amounts of both intracellular and secreted alpha-gal A
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