{"symbol":"FOXP3","synonyms":["DIETER","AIID","IPEX","JM2","XPID","PIDX"],"name":"forkhead box P3","description":"The protein encoded by this gene is a member of the forkhead/winged-helix family of transcriptional regulators. Defects in this gene are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), also known as X-linked autoimmunity-immunodeficiency syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]","ncbiEntrezGeneId":50943,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/50943","proteins":[{"symbol":"FOXP3_HUMAN","href":"/api/1.0/protein/FOXP3_HUMAN"}],"hgncRootFamilies":[{"name":"Forkhead boxes (FOX)","href":"/api/1.0/gene_family/Forkhead+boxes+%28FOX%29"}]}