SLC17A9

SLC17A9

SLC17A9

Protein-coding gene in the species Homo sapiens

Solute carrier family 17 member 9 is a protein that in humans is encoded by the SLC17A9 gene. [5]

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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

  1. [1]
    GRCh38: Ensembl release 89: ENSG00000101194 – Ensembl, May 2017
  2. [2]
    GRCm38: Ensembl release 89: ENSMUSG00000023393 – Ensembl, May 2017
  3. [3]
    "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. [4]
    "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. [5]
    "Entrez Gene: Solute carrier family 17 member 9". Retrieved 2016-07-27.

Further reading

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


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This article uses material from the Wikipedia article SLC17A9, and is written by contributors. Text is available under a CC BY-SA 4.0 International License; additional terms may apply. Images, videos and audio are available under their respective licenses.