COXFA4L3

COXFA4L3
Identifiers
AliasesCOXFA4L3, FOAP-11, NMES1, chromosome 15 open reading frame 48, MIR147BHG, MISTRAV, MOCCI, C15orf48, Cytochrome C Oxidase Associated Subunit FA4L3
External IDsOMIM: 608409; MGI: 3034182; GeneCards: COXFA4L3
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez

84419

433470

Ensembl

ENSG00000166920

ENSMUSG00000033213

UniProt

Q9C002

Q810Q5

RefSeq (mRNA)

NM_197955
NM_032413

NM_001004174

RefSeq (protein)

NP_115789
NP_922946
NP_115789.1
NP_922946.1

NP_001004174

Location (UCSC)Chr 15: 45.43 – 45.45 MbChr 2: 122.48 – 122.48 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Cytochrome c oxidase associated subunit FA4L3 is a protein that in humans is encoded by the gene COXFA4L3 (previously C15orf48).[5] It participates in an immunoregulatory response.[6] More specifically, in response to inflammation signaling, the protein COXFA4L3 replaces the COXFA4 subunit in Cytochrome c oxidase, reducing cellular respiration in the mitochondria.[6]

Function

This gene was first identified in a study of human esophageal squamous cell carcinoma tissues. Levels of both the message and protein are reduced in carcinoma samples. In adult human tissues, this gene is expressed in the esophagus, stomach, small intestine, colon and placenta. Alternatively spliced transcript variants that encode the same protein have been identified.[5]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000166920 – Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000033213 – 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 "Entrez Gene: Chromosome 15 open reading frame 48". Retrieved 2017-10-09.
  6. 1 2 "Q9C002 · CX4L3_HUMAN". uniprot.org. UniProt consortium. Retrieved 2026-07-28.

Further reading


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