- 商品货号:G100805
- accession:NM_017528
- 基因别名:WBSCR22
- 基因描述:Homo sapiens Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 2, mRNA.
- 载体:现货载体
- CDS区长度:846
- 翻译后氨基酸长度:281
- TranscriptVariant:This variant (2) lacks an exon in the 3' coding region but maintains the reading frame, compared to variant 1. The encoded isoform (2) is shorter than isoform 1.
- 基因简介: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]
- 规格:10ul 质粒
CDS区参考序列: 点击查看序列翻译后氨基酸参数序列: 点击查看序列