MGP Database

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MGP003268

Ontology/Pathway Information

Entrez Gene ID7367
Gene NameUDP glucuronosyltransferase 2 family, polypeptide B17
Gene Symbol UGT2B17
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005789 IEA:UniProtKB-SubCellCendoplasmic reticulum membrane
GO:0016021 IEA:UniProtKB-KWCintegral component of membrane
GO:0043231 IBA:GO_CentralCintracellular membrane-bounded organelle
GO:0016020 TAS:ProtIncCmembrane
GO:0015020 IDA:UniProtKBFglucuronosyltransferase activity
GO:0052695 IDA:UniProtKBPcellular glucuronidation
GO:0032870 IBA:GO_CentralPcellular response to hormone stimulus
GO:0009813 IBA:GO_CentralPflavonoid biosynthetic process
GO:0052696 IBA:GO_CentralPflavonoid glucuronidation
GO:0008202 TAS:ProtIncPsteroid metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_13433Biological oxidations
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_6784Glucuronidation
REACT_267615Metabolic disorders of biological oxidation enzymes
REACT_111217Metabolism
REACT_6959Phase II conjugation
SMP Pathway Links
SMP IDDescription
SMP0035617-Beta Hydroxysteroid Dehydrogenase III Deficiency
SMP00068Androgen and Estrogen Metabolism
SMP00565Aromatase deficiency
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