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SLC17A8, solute carrier family 17 member 8

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SLC17A8, solute carrier family 17 member 8

  • This gene encodes a vesicular glutamate transporter. The encoded protein transports the neurotransmitter glutamate into synaptic vesicles before it is released into the synaptic cleft. Mutations in this gene are the cause of autosomal-dominant nonsyndromic type 25 deafness. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]

  • Gene Synonyms (vesicular glutamate transporter 3, solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8, solute carrier family 17 (vesicular glutamate transporter), member 8, DFNA25, VGLUT3,)
  • NCBI Gene ID: 246213
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q8NDX2
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

solute carrier family 17 member 8 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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