SLC22A24

Solute carrier family 22 member 24 is a protein that in humans is encoded by the SLC22A24 gene.[5]

SLC22A24
Identifiers
AliasesSLC22A24, NET46, solute carrier family 22 member 24
External IDsOMIM: 611698 MGI: 2442751 HomoloGene: 133125 GeneCards: SLC22A24
Gene location (Human)
Chr.Chromosome 11 (human)[1]
Band11q12.3Start63,079,940 bp[1]
End63,144,221 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

283238

207151

Ensembl

ENSG00000197658

ENSMUSG00000024757

UniProt

Q8N4F4

Q8VCA0

RefSeq (mRNA)

NM_001136506
NM_173586

NM_144785

RefSeq (protein)

NP_001129978
NP_775857

NP_659034

Location (UCSC)Chr 11: 63.08 – 63.14 MbChr 19: 7.67 – 7.71 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

SLC22A24 belongs to a large family of transmembrane proteins that function as uniporters, symporters, and antiporters to transport organic ions across cell membranes (Jacobsson et al., 2007 [PubMed 17714910]).

References

  1. GRCh38: Ensembl release 89: ENSG00000197658 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000024757 - 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. "Entrez Gene: Solute carrier family 22 member 24". Retrieved 2016-04-01.

Further reading

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


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