MGP Database

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MGP003480

Ontology/Pathway Information

Entrez Gene ID8309
Gene Nameacyl-CoA oxidase 2, branched chain
Gene Symbol ACOX2
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005782 TAS:ReactomeCperoxisomal matrix
GO:0005777 IDA:UniProtKBCperoxisome
GO:0033791 IEA:UniProtKB-ECF3alpha,7alpha,12alpha-trihydroxy-5beta-cholestanoyl-CoA 24-hydroxylase activity
GO:0003995 IEA:InterProFacyl-CoA dehydrogenase activity
GO:0003997 TAS:ReactomeFacyl-CoA oxidase activity
GO:0050660 IEA:InterProFflavin adenine dinucleotide binding
GO:0016402 TAS:ReactomeFpristanoyl-CoA oxidase activity
GO:0005102 IPI:UniProtKBFreceptor binding
GO:0006699 TAS:ReactomePbile acid biosynthetic process
GO:0008206 TAS:ReactomePbile acid metabolic process
GO:0044255 TAS:ReactomePcellular lipid metabolic process
GO:0033540 TAS:ReactomePfatty acid beta-oxidation using acyl-CoA oxidase
GO:0044281 TAS:ReactomePsmall molecule metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_17017Beta-oxidation of pristanoyl-CoA
REACT_11040Bile acid and bile salt metabolism
REACT_111217Metabolism
REACT_22258Metabolism of lipids and lipoproteins
REACT_16957Peroxisomal lipid metabolism
REACT_11054Synthesis of bile acids and bile salts
REACT_11041Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol
SMP Pathway Links
SMP IDDescription
SMP0072027-Hydroxylase Deficiency
SMP00035Bile Acid Biosynthesis
SMP00315Cerebrotendinous Xanthomatosis (CTX)
SMP00314Congenital Bile Acid Synthesis Defect Type II
SMP00318Congenital Bile Acid Synthesis Defect Type III
SMP00317Familial Hypercholanemia (FHCA)
SMP00316Zellweger Syndrome
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