Your search for "wbscr22" returned 68 TaqMan® SNP Genotyping Assays
Williams-Beuren syndrome chromosome region 22
This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011]
Please enter the information below and press OK to send your cart to Core Services for purchase.