COXFA4L2

COXFA4L2
Identifiers
AliasesCOXFA4L2, NUOMS, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 4-like 2, NDUFA4, mitochondrial complex associated like 2, NDUFA4 mitochondrial complex associated like 2, MISTRH, NDUFA4L2
External IDsMGI: 3039567; GeneCards: COXFA4L2
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez

56901

407790

Ensembl

ENSG00000185633

ENSMUSG00000040280

UniProt

Q9NRX3

Q4FZG9

RefSeq (mRNA)

NM_020142
NM_001394960
NM_001394961

NM_001098789

RefSeq (protein)

NP_064527

NP_001092259

Location (UCSC)Chr 12: 57.23 – 57.24 MbChr 10: 127.35 – 127.35 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Cytochrome c oxidase hypoxia associated subunit FA4L2 is a protein that in humans is encoded by the COXFA4L2 gene (previously NDUFA4L2). COXFA4L2 is a mitochondrial protein that inhibits and regulates the electron transport chain, and is involved in the cellular response to hypoxia.

Structure

The COXFA4L2 gene is located on the long q arm of chromosome 12 at position 13.3 and it spans 5,860 base pairs.

See also

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000185633 – Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000040280 – Ensembl, 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. 1 2 3 "Entrez Gene: NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 4-like 2".

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