NSUN5 蛋白
(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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4 results
NSUN5
宿主: 人
宿主: 大肠杆菌（E. Coli）
Recombinant
Greater than 85 % as determined by SDS-PAGE.
ELISA, WB
NSUN5
宿主: 人
宿主: Insect cells (Sf9)
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliases for NSUN5 蛋白
NOP2/Sun RNA methyltransferase family member 5 (Nsun5) 蛋白NOP2/Sun domain family, member 5 (nsun5) 蛋白
NOP2/Sun RNA methyltransferase family member 5 (NSUN5) 蛋白
NOP2/Sun RNA methyltransferase family member 5 (nsun5) 蛋白
NOL1/NOP2/Sun domain family, member 5 (Nsun5) 蛋白
9830109N13Rik 蛋白
AI326939 蛋白
NOL1 蛋白
Nol1r 蛋白
NOL1R 蛋白
NSUN5A 蛋白
p120 蛋白
RGD1309268 蛋白
Wbscr20 蛋白
WBSCR20 蛋白
Wbscr20a 蛋白
WBSCR20A 蛋白
wu:fc49f12 蛋白
zgc:66176 蛋白
zgc:77183 蛋白
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