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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC17A8-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC17A8-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC17A8-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC17A8-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC17A8-20-AQ | 20 (40 μL) | 200 μL |  |
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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 Symbol : SLC17A8
Gene Name : Solute carrier family 17 member 8
Chromosome : CHR 12: 100,357,078-100,422,058
Locus : 12q23.1
Alt. Genes : ZNF263
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