Mitochondrial elongation factor 2

Jump to navigation Jump to search
VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Mitochondrial elongation factor 2 is a protein that in humans is encoded by the MIEF2 gene. [1]

Function

This gene encodes an outer mitochondrial membrane protein that functions in the regulation of mitochondrial morphology. It can directly recruit the fission mediator dynamin-related protein 1 (Drp1) to the mitochondrial surface. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011].

References

  1. "Entrez Gene: Mitochondrial elongation factor 2". Retrieved 2018-04-01.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


Template:Gene-CHR HSCHR17 3 CTG1-stub