Search results for abx031474

Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody, Abbexa, abx031474

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.