Solute carrier family 22 member 7 is a protein that in humans is encoded by the gene SLC22A7.[5][6][7]
SLC22A7 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
Aliases | SLC22A7, NLT, OAT2, solute carrier family 22 member 7, hOAT11 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 604995; MGI: 1859559; HomoloGene: 21328; GeneCards: SLC22A7; OMA:SLC22A7 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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The protein encoded by this gene is involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and appears to be localized to the basolateral membrane of the kidney. Alternatively spliced transcript variants encoding different isoforms have been described.[7]
Interactive pathway map
Click on genes, proteins and metabolites below to link to respective articles.[§ 1]
Fluorouracil (5-FU) Activity edit
See also
- SLC22A7+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
References
Further reading
This article incorporates text from the United States National Library of Medicine, which is in the public domain.