MGP Database

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MGP004341

Ontology/Pathway Information

Entrez Gene ID10720
Gene NameUDP glucuronosyltransferase 2 family, polypeptide B11
Gene Symbol UGT2B11
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:0015020 IBA:GO_CentralFglucuronosyltransferase activity
GO:0032870 IBA:GO_CentralPcellular response to hormone stimulus
GO:0008210 TAS:ProtIncPestrogen metabolic process
GO:0009813 IBA:GO_CentralPflavonoid biosynthetic process
GO:0052696 IBA:GO_CentralPflavonoid glucuronidation
GO:0006805 TAS:ProtIncPxenobiotic 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
SMP00344Acute Intermittent Porphyria
SMP00068Androgen and Estrogen Metabolism
SMP00565Aromatase deficiency
SMP00345Congenital Erythropoietic Porphyria (CEP) or Gunther Disease
SMP00553Glycogenosis, Type III. Cori disease, Debrancher glycogenosis
SMP00554Glycogenosis, Type IV. Amylopectinosis, Anderson disease
SMP00555Glycogenosis, Type VI. Hers disease
SMP00552Glycogen synthetase deficiency
SMP00342Hereditary Coproporphyria (HCP)
SMP00556Mucopolysaccharidosis VI. Sly syndrome
SMP00346Porphyria Variegata (PV)
SMP00024Porphyrin Metabolism
SMP00058Starch and Sucrose Metabolism
SMP00557Sucrase-isomaltase deficiency
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