MGP Database

New search | Record Overview | Ontology/Pathway Information | Domain Information | UniProt Annotations | Related Proteins
MGP004717

Ontology/Pathway Information

Entrez Gene ID23600
Gene Namealpha-methylacyl-CoA racemase
Gene Symbol AMACR
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005737 IDA:UniProtKBCcytoplasm
GO:0005739 IDA:UniProtKBCmitochondrion
GO:0005782 TAS:ReactomeCperoxisomal matrix
GO:0005777 IDA:UniProtKBCperoxisome
GO:0008111 IDA:UniProtKBFalpha-methylacyl-CoA racemase activity
GO:0005102 IPI:UniProtKBFreceptor binding
GO:0006699 TAS:ReactomePbile acid biosynthetic process
GO:0008206 IDA:UniProtKBPbile 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_11053Synthesis of bile acids and bile salts via 24-hydroxycholesterol
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
  logo