MGP Database

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MGP000311

Ontology/Pathway Information

Entrez Gene ID635
Gene Namebetaine--homocysteine S-methyltransferase
Gene Symbol BHMT
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005737 IDA:HPACcytoplasm
GO:0005829 TAS:ReactomeCcytosol
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0043234 IEA:EnsemblCprotein complex
GO:0047150 NAS:UniProtKBFbetaine-homocysteine S-methyltransferase activity
GO:0008898 IEA:InterProFS-adenosylmethionine-homocysteine S-methyltransferase activity
GO:0008270 IDA:BHF-UCLFzinc ion binding
GO:0006579 IEA:UniProtKB-UniPathwayPamino-acid betaine catabolic process
GO:0006577 IDA:BHF-UCLPamino-acid betaine metabolic process
GO:0034641 TAS:ReactomePcellular nitrogen compound metabolic process
GO:0071267 IDA:BHF-UCLPL-methionine salvage
GO:0006479 NAS:UniProtKBPprotein methylation
GO:0050666 NAS:UniProtKBPregulation of homocysteine metabolic process
GO:0010243 IEA:EnsemblPresponse to organonitrogen compound
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0000096 TAS:ReactomePsulfur amino acid metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_111217Metabolism
REACT_13Metabolism of amino acids and derivatives
REACT_115639Sulfur amino acid metabolism
SMP Pathway Links
SMP IDDescription
SMP007213-Phosphoglycerate dehydrogenase deficiency
SMP00123Betaine Metabolism
SMP00177Cystathionine Beta-Synthase Deficiency
SMP00179Dihydropyrimidine Dehydrogenase Deficiency (DHPD)
SMP00242Dimethylglycine Dehydrogenase Deficiency
SMP00484Dimethylglycinuria
SMP00004Glycine and Serine Metabolism
SMP00222Glycine N-methyltransferase Deficiency
SMP00570Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type
SMP00485Hyperglycinemia, non-ketotic
SMP00341Hypermethioninemia
SMP00221Methionine Adenosyltransferase Deficiency
SMP00033Methionine Metabolism
SMP00340Methylenetetrahydrofolate Reductase Deficiency (MTHFRD)
SMP00223Non Ketotic Hyperglycinemia
SMP00214S-Adenosylhomocysteine (SAH) Hydrolase Deficiency
SMP00244Sarcosinemia
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