MGP Database

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MGP000786

Ontology/Pathway Information

Entrez Gene ID1610
Gene NameD-amino-acid oxidase
Gene Symbol DAO
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005829 IDA:UniProtKBCcytosol
GO:0005782 TAS:ReactomeCperoxisomal matrix
GO:0005778 IDA:UniProtKBCperoxisomal membrane
GO:0005777 IDA:UniProtKBCperoxisome
GO:0048037 IDA:UniProtKBFcofactor binding
GO:0003884 IDA:UniProtKBFD-amino-acid oxidase activity
GO:0071949 IDA:UniProtKBFFAD binding
GO:0046983 IDA:UniProtKBFprotein dimerization activity
GO:0005102 IPI:UniProtKBFreceptor binding
GO:0034641 TAS:ReactomePcellular nitrogen compound metabolic process
GO:0055130 IDA:UniProtKBPD-alanine catabolic process
GO:0042416 IDA:UniProtKBPdopamine biosynthetic process
GO:0036088 IDA:UniProtKBPD-serine catabolic process
GO:0070178 IDA:UniProtKBPD-serine metabolic process
GO:0046487 TAS:ReactomePglyoxylate metabolic process
GO:0006551 IEA:EnsemblPleucine metabolic process
GO:0006562 IDA:UniProtKBPproline catabolic process
GO:0044281 TAS:ReactomePsmall molecule metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_16925Glyoxylate metabolism
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
SMP00036D-Arginine and D-Ornithine Metabolism
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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