MGP Database

MGP007047

Ontology/Pathway Information

Entrez Gene ID	348158
Gene Name	acyl-CoA synthetase medium-chain family member 2B
Gene Symbol	ACSM2B
Species	Homo sapiens

Gene Ontology (GO Annotations)

GO ID	Source	Type	Description
GO:0005759	TAS:Reactome	C	mitochondrial matrix
GO:0005739	NAS:BHF-UCL	C	mitochondrion
GO:0005524	IEA:UniProtKB-KW	F	ATP binding
GO:0047760	IEA:UniProtKB-EC	F	butyrate-CoA ligase activity
GO:0046872	IEA:UniProtKB-KW	F	metal ion binding
GO:0006631	IEA:UniProtKB-KW	P	fatty acid metabolic process
GO:0044281	TAS:Reactome	P	small molecule metabolic process
GO:0006805	TAS:Reactome	P	xenobiotic metabolic process

REACTOME Pathway Links

REACTOME Pathway ID	Description
REACT_6971	Amino Acid conjugation
REACT_13433	Biological oxidations
REACT_6933	Conjugation of benzoate with glycine
REACT_6889	Conjugation of carboxylic acids
REACT_6800	Conjugation of phenylacetate with glutamine
REACT_6812	Conjugation of salicylate with glycine
REACT_268587	Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD)
REACT_268321	Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD)
REACT_268129	Defective GGT1 causes Glutathionuria (GLUTH)
REACT_267887	Defective GSS causes Glutathione synthetase deficiency (GSS deficiency)
REACT_268063	Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD)
REACT_268256	Defective OPLAH causes 5-oxoprolinase deficiency (OPLAHD)
REACT_267818	Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD)
REACT_268027	Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency)
REACT_268058	Defective UGT1A1 causes hyperbilirubinemia
REACT_268618	Defective UGT1A4 causes hyperbilirubinemia
REACT_116125	Disease
REACT_267615	Metabolic disorders of biological oxidation enzymes
REACT_111217	Metabolism
REACT_6959	Phase II conjugation

SMP Pathway Links

SMP ID	Description
SMP00126	Phenylacetate Metabolism