人 WBSCR22 (NM_001202560) cDNA克隆

Accession: NM_001202560
基因名称: WBSCR22
基因别名: WBMT; MERM1; PP3381; HUSSY-3; HASJ4442
基因描述: Homo sapiens Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 1, mRNA.
种属: Human
CDS区长度: 897 (查看编码区序列)
翻译后氨基酸长度: 298 (查看氨基酸序列)
Transcript Variant: This variant (1) encodes the longer isoform (1).
产品编号 产品名称 载体 规格 价格
G100806 人 WBSCR22 (NM_001202560) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011]