人 WBSCR27 (NM_152559) cDNA克隆

Accession: NM_152559
基因名称: WBSCR27
基因描述: Homo sapiens Williams Beuren syndrome chromosome region 27 (WBSCR27), mRNA.
种属: Human
CDS区长度: 738 (查看编码区序列)
翻译后氨基酸长度: 245 (查看氨基酸序列)
产品编号 产品名称 载体 规格 价格
G132442 人 WBSCR27 (NM_152559) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008]