{"symbol":"WDR62","synonyms":["C19ORF14","MCPH2"],"name":"WD repeat domain 62","description":"This gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly, cortical malformations, and cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2011]","ncbiEntrezGeneId":284403,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/284403","proteins":[{"symbol":"WDR62_HUMAN","href":"/api/1.0/protein/WDR62_HUMAN"}],"hgncRootFamilies":[{"name":"WD repeat domain containing (WDR)","href":"/api/1.0/gene_family/WD+repeat+domain+containing+%28WDR%29"}]}