{"symbol":"RAI2","synonyms":[],"name":"retinoic acid induced 2","description":"Retinoic acid plays a critical role in development, cellular growth, and differentiation. The specific function of this retinoic acid-induced gene has not yet been determined but it may play a role in development. The chromosomal location of this gene designates it to be a candidate for diseases such as Nance-Horan syndrome, sensorineural deafness, non-specific X-linked cognitive disability, oral-facial-digital syndrome, and Fried syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]","ncbiEntrezGeneId":10742,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/10742","proteins":[{"symbol":"RAI2_HUMAN","href":"/api/1.0/protein/RAI2_HUMAN"}],"hgncRootFamilies":[]}