{"symbol":"VSX2","synonyms":["RET1","CHX10","MCOP2","MCOPCB3","HOX10"],"name":"visual system homeobox 2","description":"This gene encodes a homeobox protein originally described as a retina-specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities. [provided by RefSeq, Oct 2009]","ncbiEntrezGeneId":338917,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/338917","proteins":[{"symbol":"VSX2_HUMAN","href":"/api/1.0/protein/VSX2_HUMAN"}],"hgncRootFamilies":[{"name":"Homeoboxes","href":"/api/1.0/gene_family/Homeoboxes"}]}