MGP Database

MGP001154

Ontology/Pathway Information

Entrez Gene ID2593
Gene Nameguanidinoacetate N-methyltransferase
Gene Symbol GAMT
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005829 TAS:ReactomeCcytosol
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0030731 IMP:UniProtKBFguanidinoacetate N-methyltransferase activity
GO:0008168 TAS:ProtIncFmethyltransferase activity
GO:0034641 TAS:ReactomePcellular nitrogen compound metabolic process
GO:0006601 IDA:UniProtKBPcreatine biosynthetic process
GO:0006600 TAS:ReactomePcreatine metabolic process
GO:0006936 TAS:ProtIncPmuscle contraction
GO:0009887 IEA:EnsemblPorgan morphogenesis
GO:0040014 IEA:EnsemblPregulation of multicellular organism growth
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0007283 IEA:EnsemblPspermatogenesis
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_813Creatine metabolism
REACT_111217Metabolism
REACT_13Metabolism of amino acids and derivatives
SMP Pathway Links
SMP IDDescription
SMP007213-Phosphoglycerate dehydrogenase deficiency
SMP00020Arginine and Proline Metabolism
SMP00362Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency)
SMP00504Creatine deficiency, guanidinoacetate methyltransferase deficiency
SMP00179Dihydropyrimidine Dehydrogenase Deficiency (DHPD)
SMP00242Dimethylglycine Dehydrogenase Deficiency
SMP00484Dimethylglycinuria
SMP00004Glycine and Serine Metabolism
SMP00188Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency)
SMP00485Hyperglycinemia, non-ketotic
SMP00506Hyperornithinemia-hyperammonemia-homocitrullinuria [HHH-syndrome]
SMP00505Hyperornithinemia with gyrate atrophy (HOGA)
SMP00361Hyperprolinemia Type I
SMP00360Hyperprolinemia Type II
SMP00507L-arginine:glycine amidinotransferase deficiency
SMP00223Non Ketotic Hyperglycinemia
SMP00363Ornithine Aminotransferase Deficiency (OAT Deficiency)
SMP00207Prolidase Deficiency (PD)
SMP00208Prolinemia Type II
SMP00244Sarcosinemia
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