MGP Database

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MGP002148

Ontology/Pathway Information

Entrez Gene ID4942
Gene Nameornithine aminotransferase
Gene Symbol OAT
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005759 TAS:ReactomeCmitochondrial matrix
GO:0005739 TAS:ProtIncCmitochondrion
GO:0004587 EXP:ReactomeFornithine-oxo-acid transaminase activity
GO:0030170 IEA:InterProFpyridoxal phosphate binding
GO:0008652 TAS:ReactomePcellular amino acid biosynthetic process
GO:0034641 TAS:ReactomePcellular nitrogen compound metabolic process
GO:0055129 IEA:UniProtKB-UniPathwayPL-proline biosynthetic process
GO:0034214 IDA:UniProtKBPprotein hexamerization
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0007601 TAS:ProtIncPvisual perception
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_238Amino acid synthesis and interconversion (transamination)
REACT_111217Metabolism
REACT_13Metabolism of amino acids and derivatives
SMP Pathway Links
SMP IDDescription
SMP00020Arginine and Proline Metabolism
SMP00362Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency)
SMP00504Creatine deficiency, guanidinoacetate methyltransferase deficiency
SMP00188Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency)
SMP00506Hyperornithinemia-hyperammonemia-homocitrullinuria [HHH-syndrome]
SMP00505Hyperornithinemia with gyrate atrophy (HOGA)
SMP00361Hyperprolinemia Type I
SMP00360Hyperprolinemia Type II
SMP00507L-arginine:glycine amidinotransferase deficiency
SMP00363Ornithine Aminotransferase Deficiency (OAT Deficiency)
SMP00207Prolidase Deficiency (PD)
SMP00208Prolinemia Type II
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