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- accession：NM_001168347
- 基因别名：NSUN5
- 基因描述：Homo sapiens NOP2/Sun domain family, member 5 (NSUN5), transcript variant 3, mRNA.
- 载体：现货载体
- CDS区长度：1413
- 翻译后氨基酸长度：470
- TranscriptVariant：This variant (3) uses an alternate splice site in the 3' coding region, which results in a frameshift, compared to variant 1. The encoded isoform (3) is longer and has a distinct C-terminus, compared to isoform 1.
- 基因简介：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]
- 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
