SLC17A9 (gene)
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External IDs | GeneCards: [1] | ||||||
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Species | Human | Mouse | |||||
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Location (UCSC) | n/a | n/a | |||||
PubMed search | n/a | n/a | |||||
Wikidata | |||||||
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Solute carrier family 17 member 9 is a protein that in humans is encoded by the SLC17A9 gene. [1]
Function
This gene encodes a member of a family of transmembrane proteins that are involved in the transport of small molecules. The encoded protein participates in the vesicular uptake, storage, and secretion of adenoside triphosphate (ATP) and other nucleotides. A mutation in this gene was found in individuals with autosomal dominant disseminated superficial actinic porokeratosis-8. Alternative splicing results in multiple transcript variants.
References
- ↑ "Entrez Gene: Solute carrier family 17 member 9". Retrieved 2016-07-27.
Further reading
- Sawada K, Echigo N, Juge N, Miyaji T, Otsuka M, Omote H, Yamamoto A, Moriyama Y (2008). "Identification of a vesicular nucleotide transporter". Proc. Natl. Acad. Sci. U.S.A. 105 (15): 5683–6. doi:10.1073/pnas.0800141105. PMC 2311367. PMID 18375752.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
This article on a gene on human chromosome 20 is a stub. You can help Wikipedia by expanding it. |