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- 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
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