Solute carrier family 22 member 15

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SLC22A15
Identifiers
Aliases SLC22A15, FLIPT1, PRO34686, solute carrier family 22 member 15
External IDs OMIM: 608275 MGI: 3607704 HomoloGene: 41263 GeneCards: SLC22A15
Gene location (Human)
Chromosome 1 (human)
Chr. Chromosome 1 (human)[1]
Chromosome 1 (human)
Genomic location for SLC22A15
Genomic location for SLC22A15
Band 1p13.1 Start 115,976,498 bp[1]
End 116,070,054 bp[1]
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_018420

NM_001039371

RefSeq (protein)

NP_060890

NP_001034460

Location (UCSC) Chr 1: 115.98 – 116.07 Mb Chr 3: 101.86 – 101.92 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Solute carrier family 22 member 15 is a protein that in humans is encoded by the SLC22A15 gene. [5]

Function

Organic ion transporters, such as SLC22A15, transport various medically and physiologically important compounds, including pharmaceuticals, toxins, hormones, neurotransmitters, and cellular metabolites. These transporters are also referred to as amphiphilic solute facilitators (ASFs).

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000163393 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000033147 - 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 15". Retrieved 2016-02-23.

Further reading

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


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