SLC22A15
Solute carrier family 22 member 15
Protein-coding gene in the species Homo sapiens
Solute carrier family 22 member 15 is a protein that in humans is encoded by the SLC22A15 gene. [5]
Quick Facts SLC22A15, Identifiers ...
SLC22A15 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | SLC22A15, FLIPT1, PRO34686, solute carrier family 22 member 15 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 608275; MGI: 3607704; HomoloGene: 41263; GeneCards: SLC22A15; OMA:SLC22A15 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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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).
- "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Entrez Gene: Solute carrier family 22 member 15". Retrieved 2016-02-23.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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