MGP Database

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MGP006441

Ontology/Pathway Information

Entrez Gene ID123263
Gene Namemitochondrial methionyl-tRNA formyltransferase
Gene Symbol MTFMT
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005739 IEA:UniProtKB-SubCellCmitochondrion
GO:0004479 IEA:UniProtKB-ECFmethionyl-tRNA formyltransferase activity
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_268551Mitochondrial translation
REACT_267634Mitochondrial translation initiation
REACT_264135Organelle biogenesis and maintenance
SMP Pathway Links
SMP IDDescription
SMP00177Cystathionine Beta-Synthase Deficiency
SMP00724Folate malabsorption, hereditary
SMP00053Folate Metabolism
SMP00222Glycine N-methyltransferase Deficiency
SMP00543Homocystinuria due to defect of N(5,10)-methylene THF deficiency
SMP00570Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type
SMP00341Hypermethioninemia
SMP00221Methionine Adenosyltransferase Deficiency
SMP00033Methionine Metabolism
SMP00432Methotrexate Action Pathway
SMP00340Methylenetetrahydrofolate Reductase Deficiency (MTHFRD)
SMP00214S-Adenosylhomocysteine (SAH) Hydrolase Deficiency
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