{"symbol":"CPXCR1","synonyms":["CT77"],"name":"CPX chromosome region, candidate 1","description":"This gene is one of several genes identified in a region of the X chromosome associated with an X-linked cleft palate (CPX) disorder. The encoded protein contains a motif similar to a motif found in zinc-finger proteins. Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]","ncbiEntrezGeneId":53336,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/53336","proteins":[{"symbol":"CPXCR_HUMAN","href":"/api/1.0/protein/CPXCR_HUMAN"}],"hgncRootFamilies":[]}