MGP Database

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MGP006443

Ontology/Pathway Information

Entrez Gene ID123876
Gene Nameacyl-CoA synthetase medium-chain family member 2A
Gene Symbol ACSM2A
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005759 IEA:UniProtKB-SubCellCmitochondrial matrix
GO:0005739 NAS:BHF-UCLCmitochondrion
GO:0005524 IEA:UniProtKB-KWFATP binding
GO:0047760 IDA:BHF-UCLFbutyrate-CoA ligase activity
GO:0046872 IEA:UniProtKB-KWFmetal ion binding
GO:0006631 IEA:UniProtKB-KWPfatty acid metabolic process
GO:0042593 NAS:BHF-UCLPglucose homeostasis
GO:0036112 IDA:BHF-UCLPmedium-chain fatty-acyl-CoA metabolic process
GO:0070328 NAS:BHF-UCLPtriglyceride homeostasis
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_6971Amino Acid conjugation
REACT_13433Biological oxidations
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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