The protein encoded by this gene is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X-linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC6A8-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC6A8-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC6A8-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC6A8-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC6A8-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X-linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
Gene Symbol : SLC6A8
Gene Name : Solute carrier family 6 member 8
Chromosome : CHR X: 153,688,296-153,696,592
Locus : Xq28
Alt. Genes : ZNF263
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