MNX1 motor neuron and pancreas homeobox 1 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 3110)
Symbol: MNX1
Full name: motor neuron and pancreas homeobox 1
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: HB9; HLXB9; HOXHB9; SCRA1
Summary: 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]
Expression: Biased expression in colon (RPKM 3.3), small intestine (RPKM 2.3) and 7 other tissues
Orthologs: mouse
Gene size: 5810bp
Exon count: 4