MGP Database

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MGP001355

Ontology/Pathway Information

Entrez Gene ID2948
Gene Nameglutathione S-transferase mu 4
Gene Symbol GSTM4
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005737 IDA:BHF-UCLCcytoplasm
GO:0005829 TAS:ReactomeCcytosol
GO:0019899 IPI:BHF-UCLFenzyme binding
GO:0043295 IDA:BHF-UCLFglutathione binding
GO:0004364 IDA:BHF-UCLFglutathione transferase activity
GO:0042803 IPI:BHF-UCLFprotein homodimerization activity
GO:1901687 TAS:ReactomePglutathione derivative biosynthetic process
GO:0006749 IDA:BHF-UCLPglutathione metabolic process
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0042178 IDA:BHF-UCLPxenobiotic catabolic process
GO:0006805 TAS:ReactomePxenobiotic 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_6926Glutathione conjugation
REACT_267615Metabolic disorders of biological oxidation enzymes
REACT_111217Metabolism
REACT_6959Phase II conjugation
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