NSUN5 抗体
(NOP2/Sun Domain Family, Member 5 (NSUN5))
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].
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Aliases for NSUN5 抗体
NOP2/Sun RNA methyltransferase family member 5 (Nsun5) 抗体NOP2/Sun domain family, member 5 (nsun5) 抗体
NOP2/Sun RNA methyltransferase family member 5 (NSUN5) 抗体
NOP2/Sun RNA methyltransferase family member 5 (nsun5) 抗体
NOL1/NOP2/Sun domain family, member 5 (Nsun5) 抗体
9830109N13Rik 抗体
AI326939 抗体
NOL1 抗体
Nol1r 抗体
NOL1R 抗体
NSUN5A 抗体
p120 抗体
RGD1309268 抗体
Wbscr20 抗体
WBSCR20 抗体
Wbscr20a 抗体
WBSCR20A 抗体
wu:fc49f12 抗体
zgc:66176 抗体
zgc:77183 抗体
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