MTFMT
Sign in to saveAlso known as COXPD15, FMT1, mitochondrial methionyl-tRNA formyltransferase, MC1DN27
Mitochondrial methionyl-tRNA formyltransferase is a protein that in humans is encoded by the MTFMT gene.
Gene data
MTFMT- Name
- mitochondrial methionyl-tRNA formyltransferase
- Type
- protein-coding
- Aliases
- COXPD15, FMT1, MC1DN27
The protein encoded by this nuclear gene localizes to the mitochondrion, where it catalyzes the formylation of methionyl-tRNA. [provided by RefSeq, Jun 2011].
via MyGene.info
Gene · Ensembl
mitochondrial methionyl-tRNA formyltransferase
- Symbol
- MTFMT
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 15:64,990,829-65,029,652
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 12320
- genomic end
- 65029639
- exact match
- identifiers.org/ncbigene/123263
- genomic start
- 65294845
- cytogenetic location
- 15q22.31
Sources (4)
via Wikidata · CC0
~1 min read
Article
2 sectionsContents
- References
- Further reading
Mitochondrial methionyl-tRNA formyltransferase is a protein that in humans is encoded by the MTFMT gene.
The protein encoded by this nuclear gene localizes to the mitochondrion, where it catalyzes the formylation of methionyl-tRNA. Recessive-type mutations in MTFMT have been shown to cause mitochondrial disease.