产品介绍 基因名： NSUN5 产品别名： NOL1； NOL1R； NSUN5A； WBSCR20； WBSCR20A； p120； p120(NOL1)； NSUN5； NOP2/Sun RNA methyltransferase 5； NOP2/Sun RNA methyltransferase 5； 28S rRNA (cytosine-C(5))-methyltransferase； NOL1-related protein； NOL1/NOP2/Sun domain family member 5； NOP2/Sun RNA methyltransferase family member 5； NOP2/Sun domain family, member 5； NOP2/Sun domain family, member 5A； Williams Beuren syndrome chromosome region 20A； Williams-Beuren syndrome chromosomal region 20A protein； Williams-Beuren syndrome critical region protein 20 copy A； probable 28S rRNA (cytosine-C(5))-methyltransferase； putative methyltransferase NSUN5； 甲基转移酶NSUN5； 背景信息： This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013] 标签：His-tag |
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