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Gene : SLC17A9 Homo sapiens

Name  ? solute carrier family 17 member 9 Cytological Location  20q13.33
Brief Description  solute carrier family 17 member 9
description  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. [provided by RefSeq, Nov 2014]
  • synonyms:
  • solute carrier family 17, member 9,
  • VNUT,
  • SLC17A9,
  • HGNC:16192,
  • C20orf59,
  • solute carrier family 17 (vesicular nucleotide transporter), member 9,
  • FLJ23412,
  • AK027065,
  • OTTHUMG00000032951,
  • NM_022082,
  • chromosome 20 open reading frame 59,
  • C20orf59,
  • uc002yea.5,
  • VNUT,
  • POROK8
  • identifiers:
  • 63910,
  • ENSG00000101194,
  • SLC17A9

Genome feature

Region: gene ? Length: 16896  
Location: 20:62952690-62969585 Cyto location: 20q13.33

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

798 SN Ps

5 Cross References

17 Data Sets

14 Homologues

0 Located Features

97 Rna Seq Results