MGP Database

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MGP003015

Ontology/Pathway Information

Entrez Gene ID6799
Gene Namesulfotransferase family, cytosolic, 1A, phenol-preferring, member 2
Gene Symbol SULT1A2
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005829 TAS:ReactomeCcytosol
GO:0004062 IDA:UniProtKBFaryl sulfotransferase activity
GO:0047894 IDA:BHF-UCLFflavonol 3-sulfotransferase activity
GO:0008146 TAS:ProtIncFsulfotransferase activity
GO:0050427 TAS:ReactomeP3'-phosphoadenosine 5'-phosphosulfate metabolic process
GO:0009309 TAS:ProtIncPamine biosynthetic process
GO:0006584 IEA:UniProtKB-KWPcatecholamine metabolic process
GO:0018958 IDA:UniProtKBPphenol-containing compound metabolic process
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0008202 IEA:UniProtKB-KWPsteroid metabolic process
GO:0051923 IDA:BHF-UCLPsulfation
GO:0006805 IDA:UniProtKBPxenobiotic metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_13433Biological oxidations
REACT_6913Cytosolic sulfonation of small molecules
REACT_268587Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD)
REACT_268321Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD)
REACT_268129Defective GGT1 causes Glutathionuria (GLUTH)
REACT_267887Defective GSS causes Glutathione synthetase deficiency (GSS deficiency)
REACT_268063Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD)
REACT_268256Defective OPLAH causes 5-oxoprolinase deficiency (OPLAHD)
REACT_267818Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD)
REACT_268027Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency)
REACT_268058Defective UGT1A1 causes hyperbilirubinemia
REACT_268618Defective UGT1A4 causes hyperbilirubinemia
REACT_116125Disease
REACT_267615Metabolic disorders of biological oxidation enzymes
REACT_111217Metabolism
REACT_6959Phase II conjugation
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