SLC17A9
Identifiers
Aliases	SLC17A9, C20orf59, VNUT, POROK8, solute carrier family 17 member 9
External IDs	OMIM: 612107 MGI: 1919107 HomoloGene: 76562 GeneCards: SLC17A9
Gene location (Human) Chr. Chromosome 20 (human)[1] Band 20q13.33 Start 62,952,707 bp[1] End 62,969,585 bp[1]
Gene location (Mouse) Chr. Chromosome 2 (mouse)[2] Band 2|2 H4 Start 180,367,056 bp[2] End 180,384,073 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in right lobe of liver stromal cell of endometrium spleen pylorus bone marrow cells body of stomach pancreatic ductal cell lymph node ascending aorta fundus Top expressed in large intestine colon molar left colon spermatocyte spleen blood yolk sac duodenum thymus More reference expression data BioGPS n/a
Gene ontology Molecular function transmembrane transporter activity transporter activity Cellular component integral component of membrane membrane Biological process anion transport transmembrane transport exocytosis Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 63910 228993 Ensembl ENSG00000101194 ENSMUSG00000023393 UniProt Q9BYT1 Q8VCL5 RefSeq (mRNA) NM_001302643 NM_022082 NM_183161 RefSeq (protein) NP_001289572 NP_071365 NP_898984 Location (UCSC) Chr 20: 62.95 – 62.97 Mb Chr 2: 180.37 – 180.38 Mb PubMed search [3] [4]
Wikidata
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Solute carrier family 17 member 9 is a protein that in humans is encoded by the SLC17A9 gene. ^[5]

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.