MGP Database

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MGP006278

Ontology/Pathway Information

Entrez Gene ID92292
Gene Nameglycine-N-acyltransferase-like 1
Gene Symbol GLYATL1
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005739 IEA:InterProCmitochondrion
GO:0047946 IEA:UniProtKB-ECFglutamine N-acyltransferase activity
GO:0047961 IEA:InterProFglycine N-acyltransferase activity
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_6971Amino Acid conjugation
REACT_13433Biological oxidations
REACT_6933Conjugation of benzoate with glycine
REACT_6889Conjugation of carboxylic acids
REACT_6812Conjugation of salicylate with glycine
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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