MGP Database

New search | Record Overview | Ontology/Pathway Information | Domain Information | UniProt Annotations | Related Proteins
MGP006367

Ontology/Pathway Information

Entrez Gene ID116285
Gene Nameacyl-CoA synthetase medium-chain family member 1
Gene Symbol ACSM1
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0072562 IDA:UniProtKBCblood microparticle
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0005759 IDA:UniProtKBCmitochondrial matrix
GO:0003996 IDA:UniProtKBFacyl-CoA ligase activity
GO:0005524 IEA:UniProtKB-KWFATP binding
GO:0047760 IDA:UniProtKBFbutyrate-CoA ligase activity
GO:0015645 IEA:EnsemblFfatty acid ligase activity
GO:0005525 IEA:UniProtKB-KWFGTP binding
GO:0046872 IEA:UniProtKB-KWFmetal ion binding
GO:0018874 NAS:UniProtKBPbenzoate metabolic process
GO:0019605 NAS:UniProtKBPbutyrate metabolic process
GO:0042632 NAS:BHF-UCLPcholesterol homeostasis
GO:0015980 NAS:UniProtKBPenergy derivation by oxidation of organic compounds
GO:0006633 IEA:EnsemblPfatty acid biosynthetic process
GO:0019395 NAS:UniProtKBPfatty acid oxidation
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0006805 TAS:ReactomePxenobiotic metabolic process
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_6800Conjugation of phenylacetate with glutamine
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
SMP Pathway Links
SMP IDDescription
SMP00073Butyrate Metabolism
SMP00481Mitochondrial Beta-Oxidation of Medium Chain Saturated Fatty Acids
SMP00126Phenylacetate Metabolism
SMP00635Valproic Acid Metabolism Pathway
  logo