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GeneQ18049530· pop 5· linked from 3 articles

Also 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.

In the Vinony graph

Within Vinony's link graph, MTFMT is referenced by 3 other articles, and connects out to PubMed, human chromosome 15 and Ensembl genome database project.

It is catalogued under topics including Genes mutated in mice and Genes on human chromosome 15.

Its subject is documented across 5 Wikipedia language editions.

Gene data

MTFMT
Name
mitochondrial methionyl-tRNA formyltransferase
Type
protein-coding
Position
64,990,829–65,029,652 (−)
Aliases
COXPD15, FMT1, MC1DN27
RefSeq RNA
NM_139242.4, XM_005254158.6, XM_054377265.1, XR_001751081.2, XR_007064421.1
RefSeq protein
NP_640335.2, XP_005254215.2, XP_054233240.1

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
View on Ensembl →

via Ensembl · EMBL-EBI

Wikidata facts

Instance of
gene
Show 7 more facts
HomoloGene ID
12320
genomic end
65029639
found in taxon
Homo sapiens
genomic start
65294845
cytogenetic location
15q22.31
Sources (4)

via Wikidata · CC0

~1 min read

Encyclopedic overview

2 sections
Contents
  • 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.

Excerpted from Wikipedia’s “MTFMT” article, available under the CC BY-SA 4.0 licence.

Available in 5 languages

via Wikidata sitelinks · CC0

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