Your search for "wbscr17" returned 1,271 TaqMan® SNP Genotyping Assays
Williams-Beuren syndrome chromosome region 17
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]
AA388321, E330012B09RIK, GALNAC-T5L, GALNACT17, GALNT16, GALNT20, GALNTL3, WBSCR17
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