MGP Database

MGP003957

Ontology/Pathway Information

Entrez Gene ID9615
Gene Nameguanine deaminase
Gene Symbol GDA
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005829 TAS:ReactomeCcytosol
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0005622 TAS:ProtIncCintracellular
GO:0008892 EXP:ReactomeFguanine deaminase activity
GO:0008270 TAS:ProtIncFzinc ion binding
GO:0006147 IEA:UniProtKB-UniPathwayPguanine catabolic process
GO:0007399 TAS:ProtIncPnervous system development
GO:0006139 TAS:ProtIncPnucleobase-containing compound metabolic process
GO:0055086 TAS:ReactomePnucleobase-containing small molecule metabolic process
GO:0006144 TAS:ReactomePpurine nucleobase metabolic process
GO:0006195 TAS:ReactomePpurine nucleotide catabolic process
GO:0044281 TAS:ReactomePsmall molecule metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_111217Metabolism
REACT_1698Metabolism of nucleotides
REACT_2086Purine catabolism
REACT_522Purine metabolism
SMP Pathway Links
SMP IDDescription
SMP00535Adenine phosphoribosyltransferase deficiency (APRT)
SMP00144Adenosine Deaminase Deficiency
SMP00167Adenylosuccinate Lyase Deficiency
SMP00168AICA-Ribosiduria
SMP00427Azathioprine Action Pathway
SMP00172Beta Ureidopropionase Deficiency
SMP00178Dihydropyrimidinase Deficiency
SMP00365Gout or Kelley-Seegmiller Syndrome
SMP00364Lesch-Nyhan Syndrome (LNS)
SMP00428Mercaptopurine Action Pathway
SMP00536Mitochondrial DNA depletion syndrome
SMP00202MNGIE (Mitochondrial Neurogastrointestinal Encephalopathy)
SMP00203Molybdenum Cofactor Deficiency
SMP00537Myoadenylate deaminase deficiency
SMP00050Purine Metabolism
SMP00210Purine Nucleoside Phosphorylase Deficiency
SMP00046Pyrimidine Metabolism
SMP00430Thioguanine Action Pathway
SMP00219UMP Synthase Deiciency (Orotic Aciduria)
SMP00220Xanthine Dehydrogenase Deficiency (Xanthinuria)
SMP00512Xanthinuria type I
SMP00513Xanthinuria type II
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