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- 商品货号：G100273
- accession：NM_004387
- 基因别名：NKX2-5
- 基因描述：Homo sapiens NK2 homeobox 5 (NKX2-5), transcript variant 1, mRNA.
- 载体：现货载体
- CDS区长度：975
- 翻译后氨基酸长度：324
- TranscriptVariant：This variant (1) represents the shortest transcript but encodes the longest isoform (1).
- 基因简介：This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
- 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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