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Proteintech
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Immunogen sequence: RNEDLLEVG SRPGPASQLP RFVRVNTLKT CSDDVVDYFK RQGFSYQGRA SSLDDLRALK GKHFLLDPLM PELLVFPAQT DLHEHPLYRA GHLILQDRAS CLPAMLLDPP PGSHVIDACA APGNKTSHLA ALLKNQGKIF AFDLDAKRLA SMATLLARAG VSCCELAEED FLAVSPSDPR YHEVHYILLD PSCSGSGMPS RQLEEPGAGT PSPVRLHALA GFQQRALCHA LTFPSLQRLV YSTCSLCQEE NEDVVRDALQ QNPGAFRLAP ALPAWPHRGL STFPGAEHCL RASPETTLSS GFFVAVIERV EVPSSASQAK ASAPERTPSP APKRKKRQQR AAAGACTPPC T (117-466 aa encoded by BC008084)
NSUN5 is a member of the evolutionarily conserved NOL1/NOP2/Sun domain family. The encoded protein may function as a DNA methyltransferase in the nucleus. The 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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: 28S rRNA (cytosine-C(5))-methyltransferase; FLJ10267; MGC986; NOL1-related protein; NOL1/NOP2/Sun domain family member 5; NOL1/NOP2/Sun domain family, member 5; NOL1R; NOP2/Sun domain family, member 5; NOP2/Sun domain family, member 5A; probable 28S rRNA (cytosine-C(5))-methyltransferase; putative methyltransferase NSUN5; Williams Beuren syndrome chromosome region 20A; Williams Beuren syndrome chromosome region 20A homolog; Williams-Beuren syndrome chromosomal region 20A protein; Williams-Beuren syndrome chromosomal region 20A protein homolog; Williams-Beuren syndrome critical region protein 20; Williams-Beuren syndrome critical region protein 20 copy A
基因别名: 9830109N13Rik; AI326939; NOL1; NOL1R; NSUN5; NSUN5A; p120; p120(NOL1); RGD1309268; WBSCR20; WBSCR20A
UniProt ID: (Human) Q96P11, (Mouse) Q8K4F6
Entrez Gene ID: (Human) 55695, (Mouse) 100609, (Rat) 288595