这个基因编码一个核蛋白,它包含一个同源盒结构域,是一个转录因子。这个基因的突变会导致咖喱子综合征,一种常染色体显性先天畸形。另外,已经发现该基因编码不同亚型的剪接转录变体[由RefSeq提供,2009年9月]
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]
基因名: | MNX1 |
别名: | HB9,HLXB9,SCRA1,HOXHB9 |
基因ID: | 3110 |
Chromosome: (GRCh37) | 7 Start: 156797547 End: 156803347 Strand: |
信号通路: |