Description
Product Characteristics:
Aliases: FLJ10267 antibody, MGC986 antibody, NOL1 antibody, NOL1-related protein antibody, NOL1/NOP2/Sun domain family member 5 antibody, NOL1R antibody, NOP2/Sun domain family, member 5 antibody, NOP2/Sun domain family, member 5A antibody, NSUN5 antibody, NSUN5_HUMAN antibody, p120 antibody, Putative methyltransferase NSUN5 antibody, WBSCR20 antibody, WBSCR20A antibody, Williams Beuren syndrome chromosome region 20A antibody, Williams-Beuren syndrome chromosomal region 20A protein antibody, Williams-Beuren syndrome critical region protein 20 copy A antibody
Target Information: This gene encodes a member of the evolutionarily conserved NOL1/NOP2/Sun domain family. The encoded protein may function as a DNA methyltransferase in the nucleus. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2009]