人 MNX1 (NM_001165255) cDNA克隆

Accession: NM_001165255
基因名称: MNX1
基因别名: HB9; HLXB9; SCRA1; HOXHB9
基因描述: Homo sapiens motor neuron and pancreas homeobox 1 (MNX1), transcript variant 2, mRNA.
种属: Human
CDS区长度: 570 (查看编码区序列)
翻译后氨基酸长度: 189 (查看氨基酸序列)
Transcript Variant: 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.
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G148351 人 MNX1 (NM_001165255) cDNA克隆 pDONR223 2ug质粒 点击询价

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]