| 1309462 | Mtfmt | mitochondrial methionyl-tRNA formyltransferase | ENCODES a protein that exhibits methionyl-tRNA formyltransferase activity (ortholog); INVOLVED IN conversion of methionyl-tRNA to N-formyl-methionyl-tRNA (ortholog); PARTICIPATES IN folate metabolic pathway; glycine N-methyltransferase deficiency pathway; hereditary folate malabsorption pathway; ASS OCIATED WITH combined oxidative phosphorylation deficiency 15 (ortholog); Dwarfism (ortholog); genetic disease (ortholog); FOUND IN mitochondrion (ortholog); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 2,4-dinitrotoluene; 2,6-dinitrotoluene | 8 | 74848936 | 74866987 | Rat | 85 | symbol , PhenoGen | gene, protein-coding, PROVISIONAL [RefSeq] |
| 1553284 | Mtfmt | mitochondrial methionyl-tRNA formyltransferase | Predicted to enable methionyl-tRNA formyltransferase activity. Predicted to be involved in conversion of methionyl-tRNA to N-formyl-methionyl-tRNA. Located in mitochondrion. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 15 and nuclear type mitochondrial c omplex I deficiency 27. Orthologous to human MTFMT (mitochondrial methionyl-tRNA formyltransferase). [provided by Alliance of Genome Resources, Jul 2025] | 9 | 65343064 | 65360336 | Mouse | 102 | symbol , PhenoGen , description | gene, protein-coding, VALIDATED [RefSeq] |
| 1604246 | MTFMT | mitochondrial methionyl-tRNA formyltransferase | The protein encoded by this nuclear gene localizes to the mitochondrion, where it catalyzes the formylation of methionyl-tRNA. [provided by RefSeq, Jun 2011] | 15 | 65001512 | 65029639 | Human | 155 | symbol , COSMIC , Human Proteome Map | gene, protein-coding, REVIEWED [RefSeq] |
| 8935739 | Mtfmt | mitochondrial methionyl-tRNA formyltransferase | ENCODES a protein that exhibits methionyl-tRNA formyltransferase activity (ortholog); INVOLVED IN conversion of methionyl-tRNA to N-formyl-methionyl-tRNA (ortholog); PARTICIPATES IN folate metabolic pathway; glycine N-methyltransferase deficiency pathway; hereditary folate malabsorption pathway; ASS OCIATED WITH combined oxidative phosphorylation deficiency 15 (ortholog); Dwarfism (ortholog); genetic disease (ortholog); FOUND IN mitochondrion (ortholog) | NW_004955450 | 10399472 | 10415813 | Chinchilla | 22 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 11917642 | MTFMT | mitochondrial methionyl-tRNA formyltransferase | ENCODES a protein that exhibits catalytic activity (inferred); methionyl-tRNA formyltransferase activity (inferred); transferase activity (inferred); INVOLVED IN conversion of methionyl-tRNA to N-formyl-methionyl-tRNA (inferred); translation (inferred); translational initiation (inferred); PARTICIPA TES IN folate metabolic pathway; glycine N-methyltransferase deficiency pathway; hereditary folate malabsorption pathway; ASSOCIATED WITH combined oxidative phosphorylation deficiency 15 (ortholog); Dwarfism (ortholog); genetic disease (ortholog); FOUND IN mitochondrion (inferred) | 15 | 43942227 | 43969182 | Bonobo | 32 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 12402656 | MTFMT | mitochondrial methionyl-tRNA formyltransferase | ENCODES a protein that exhibits catalytic activity (inferred); GTP binding (inferred); GTPase activity (inferred); INVOLVED IN conversion of methionyl-tRNA to N-formyl-methionyl-tRNA (inferred); translation (inferred); translational initiation (inferred); PARTICIPATES IN folate metabolic pathway; gl ycine N-methyltransferase deficiency pathway; hereditary folate malabsorption pathway; ASSOCIATED WITH combined oxidative phosphorylation deficiency 15 (ortholog); Dwarfism (ortholog); genetic disease (ortholog); FOUND IN mitochondrion (inferred) | 30 | 29388600 | 29415578 | Dog | 36 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 12438702 | Mtfmt | mitochondrial methionyl-tRNA formyltransferase | ENCODES a protein that exhibits catalytic activity (inferred); methionyl-tRNA formyltransferase activity (inferred); transferase activity (inferred); INVOLVED IN conversion of methionyl-tRNA to N-formyl-methionyl-tRNA (inferred); translation (inferred); translational initiation (inferred); PARTICIPA TES IN folate metabolic pathway; glycine N-methyltransferase deficiency pathway; hereditary folate malabsorption pathway; ASSOCIATED WITH combined oxidative phosphorylation deficiency 15 (ortholog); Dwarfism (ortholog); genetic disease (ortholog); FOUND IN mitochondrion (inferred) | NW_004936471 | 25334544 | 25352520 | Squirrel | 32 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 13852063 | MTFMT | mitochondrial methionyl-tRNA formyltransferase | ENCODES a protein that exhibits catalytic activity (inferred); methionyl-tRNA formyltransferase activity (inferred); transferase activity (inferred); INVOLVED IN conversion of methionyl-tRNA to N-formyl-methionyl-tRNA (inferred); translation (inferred); translational initiation (inferred); PARTICIPA TES IN folate metabolic pathway; glycine N-methyltransferase deficiency pathway; hereditary folate malabsorption pathway; ASSOCIATED WITH combined oxidative phosphorylation deficiency 15 (ortholog); Dwarfism (ortholog); genetic disease (ortholog); FOUND IN mitochondrion (inferred); INTERACTS WITH deoxynivalenol | | | | Pig | 33 | symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 18640813 | MTFMT | mitochondrial methionyl-tRNA formyltransferase | ENCODES a protein that exhibits catalytic activity (inferred); methionyl-tRNA formyltransferase activity (inferred); transferase activity (inferred); INVOLVED IN conversion of methionyl-tRNA to N-formyl-methionyl-tRNA (inferred); translation (inferred); translational initiation (inferred); PARTICIPA TES IN folate metabolic pathway; glycine N-methyltransferase deficiency pathway; hereditary folate malabsorption pathway; ASSOCIATED WITH combined oxidative phosphorylation deficiency 15 (ortholog); Dwarfism (ortholog); genetic disease (ortholog); FOUND IN mitochondrion (inferred) | | | | Green Monkey | 32 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 625869683 | Mtfmt | mitochondrial methionyl-tRNA formyltransferase | ENCODES a protein that exhibits methionyl-tRNA formyltransferase activity (ortholog); INVOLVED IN conversion of methionyl-tRNA to N-formyl-methionyl-tRNA (ortholog); PARTICIPATES IN folate metabolic pathway; glycine N-methyltransferase deficiency pathway; hereditary folate malabsorption pathway; ASS OCIATED WITH combined oxidative phosphorylation deficiency 15 (ortholog); Dwarfism (ortholog); genetic disease (ortholog); FOUND IN mitochondrion (ortholog) | | | | Black Rat | 22 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 18918393 | Mtfmt | mitochondrial methionyl-tRNA formyltransferase | ENCODES a protein that exhibits catalytic activity (inferred); methionyl-tRNA formyltransferase activity (inferred); transferase activity (inferred); INVOLVED IN conversion of methionyl-tRNA to N-formyl-methionyl-tRNA (inferred); translation (inferred); translational initiation (inferred); PARTICIPA TES IN folate metabolic pathway; glycine N-methyltransferase deficiency pathway; hereditary folate malabsorption pathway; ASSOCIATED WITH combined oxidative phosphorylation deficiency 15 (ortholog); Dwarfism (ortholog); genetic disease (ortholog); FOUND IN mitochondrion (inferred) | | | | Naked Mole-Rat | 30 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 155244015 | mtfmt | | | | | | Tropical Clawed Frog | | symbol | gene, null |
| 155250040 | mtfmt.L | | | | | | African Clawed Frog | | symbol | gene, null |