NSUN5 Products

Description

NSUN5 encodes a protein with similarity to p120 (NOL1), a 120-kDa proliferation-associated nucleolar antigen that is a member of an evolutionarily conserved protein family. 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 two transcript variants encoding different isoforms. [provided by RefSeq]

Bioinformatics

Uniprot	NM_148956 Human NP_060514.1 Human Q96P11 Human
Product By Gene ID	55695
Alternate Names	EC 2.1.1.- FLJ10267 member 5A MGC986 NOL1 NOL1/NOP2/Sun domain family member 5 NOL1/NOP2/Sun domain family, member 5 NOL1R(NOL1) NOL1-related protein NOP2/Sun domain family, member 5 NSUN5A p120 putative methyltransferase NSUN5 WBSCR20 WBSCR20A Williams-Beuren syndrome chromosomal region 20A protein Williams-Beuren syndrome critical region protein 20 copy A Ynl022cL