- accession:NM_148956
- 基因别名:NSUN5
- 基因描述:Homo sapiens NOP2/Sun domain family, member 5 (NSUN5), transcript variant 1, mRNA.
- 载体: 现货载体
- CDS区长度:1401
- 翻译后氨基酸长度:466
- TranscriptVariant:This variant (1) encodes 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]
- 载体信息:自有图片地址
- 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