Mitochondrial dynamics protein MID49

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Josvebot (talk | contribs) at 07:53, 27 July 2018 (→‎Further reading: Fixing WP:CHECKWIKI #16: unicode contol character (and other minor general edits caused by AWB), replaced: →). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

MIEF2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMIEF2, SMCR7, mitochondrial elongation factor 2, MID49, COXPD49
External IDsOMIM: 615498; MGI: 2144199; HomoloGene: 27354; GeneCards: MIEF2; OMA:MIEF2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_148886
NM_001144900
NM_139162

NM_001009927

RefSeq (protein)

NP_001138372
NP_631901
NP_683684

NP_001009927

Location (UCSC)Chr 17: 18.26 – 18.27 MbChr 11: 60.62 – 60.62 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Mitochondrial elongation factor 2 is a protein that in humans is encoded by the MIEF2 gene. [5]

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. ^ a b c ENSG00000177427 GRCh38: Ensembl release 89: ENSG00000284495, ENSG00000177427Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000018599Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "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