人 MNX1 (NM_005515) cDNA克隆

Accession: NM_005515
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 1, mRNA.
种属: Human
CDS区长度: 1206 (查看编码区序列)
翻译后氨基酸长度: 401 (查看氨基酸序列)
Transcript Variant: This variant (1) encodes the longer isoform (1).
产品编号 产品名称 载体 规格 价格
G148352 人 MNX1 (NM_005515) 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]