Solute carrier family 22 member 15

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

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

AliasesSLC22A15, FLIPT1, PRO34686, solute carrier family 22 member 15
End116,070,054 bp[1]
Quick facts SLC22A15, Identifiers ...
SLC22A15
Identifiers
AliasesSLC22A15, FLIPT1, PRO34686, solute carrier family 22 member 15
External IDsOMIM: 608275; MGI: 3607704; HomoloGene: 41263; GeneCards: SLC22A15; OMA:SLC22A15 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_018420

NM_001039371

RefSeq (protein)

NP_060890

NP_001034460

Location (UCSC)Chr 1: 115.98 – 116.07 MbChr 3: 101.86 – 101.92 Mb
PubMed search[3][4]
Wikidata
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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

Further reading

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