{"symbol":"MNX1","synonyms":["HLXB9","SCRA1","HB9","HOXHB9"],"name":"motor neuron and pancreas homeobox 1","description":"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]","ncbiEntrezGeneId":3110,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/3110","proteins":[{"symbol":"MNX1_HUMAN","href":"/api/1.0/protein/MNX1_HUMAN"}],"hgncRootFamilies":[{"name":"Homeoboxes","href":"/api/1.0/gene_family/Homeoboxes"}]}