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- accession：NM_001165255
- 基因别名：MNX1
- 基因描述：Homo sapiens motor neuron and pancreas homeobox 1 (MNX1), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：570
- 翻译后氨基酸长度：189
- TranscriptVariant：This variant (2) has an alternate 5' exon, as compared to variant 1. The resulting isoform (2) is shorter and has a distinct N-terminus, as compared to isoform 1.
- 基因简介：This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 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
