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

SLC17A9
Identifiers
AliasesSLC17A9, C20orf59, VNUT, POROK8, solute carrier family 17 member 9
External IDsOMIM: 612107; MGI: 1919107; HomoloGene: 76562; GeneCards: SLC17A9; OMA:SLC17A9 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001302643
NM_022082

NM_183161

RefSeq (protein)

NP_001289572
NP_071365

NP_898984

Location (UCSC)Chr 20: 62.95 – 62.97 MbChr 2: 180.37 – 180.38 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

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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

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000101194Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000023393Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: Solute carrier family 17 member 9". Retrieved 2016-07-27.

Further reading

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