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]
应用类型
WB
免疫原
Recombinant fusion protein of human MNX1/HB9/HLXB9(NP_005506.3).
