This gene encodes an N-acetylgalactosaminyltransferase. This gene is located centromeric to the common deleted region in Williams-Beuren syndrome (WBS), a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. This protein may play a role in membrane trafficking. [provided by RefSeq, Jan 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| GALNT17-20-RE | 20 (40 μL) | 200 μL |  |
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| GALNT17-20-OR | 20 (40 μL) | 200 μL |  |
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| GALNT17-20-GO | 20 (40 μL) | 200 μL |  |
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| GALNT17-20-GR | 20 (40 μL) | 200 μL |  |
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| GALNT17-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an N-acetylgalactosaminyltransferase. This gene is located centromeric to the common deleted region in Williams-Beuren syndrome (WBS), a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. This protein may play a role in membrane trafficking. [provided by RefSeq, Jan 2013]
Gene Symbol : GALNT17
Gene Name : Polypeptide N-acetylgalactosaminyltransferase 17
Chromosome : CHR 7: 711,324,13-717,136,00
Locus : 7q11.22
Alt. Genes : RBM12
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