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Protein Coding Gene : Slc17a9 solute carrier family 17, member 9
Primary Identifier  MGI:1919107 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  228993
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables purine nucleotide uniporter activity. Involved in purine nucleotide import into lysosome. Acts upstream of with a positive effect on ATP export. Acts upstream of or within lysosomal protein catabolic process. Located in chromaffin granule membrane. Is active in lysosomal membrane. Is expressed in esophagus; male reproductive gland or organ; and nasal cavity epithelium. Human ortholog(s) of this gene implicated in porokeratosis. Orthologous to human SLC17A9 (solute carrier family 17 member 9).
PHENOTYPE: Homozygous knockout affects the neuroendocrine system, resulting in hypoglycemia, increased glucose tolerance and increased insulin sensitivity. [provided by MGI curators]
  • synonyms:
  • MGC:28538,
  • 1700019H03Rik,
  • MGI:2670971,
  • BC019537,
  • Slc17a9,
  • RIKEN cDNA 1700019H03 gene,
  • Vnut,
  • cDNA sequence BC019537,
  • solute carrier family 17, member 9
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