{"symbol":"SOX14","synonyms":["SOX28"],"name":"SRY (sex determining region Y)-box 14","description":"This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene are suggested to be responsible for the limb defects associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Mobius syndrome. [provided by RefSeq, Jul 2008]","ncbiEntrezGeneId":8403,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/8403","proteins":[{"symbol":"SOX14_HUMAN","href":"/api/1.0/protein/SOX14_HUMAN"}],"hgncRootFamilies":[{"name":"SRY (sex determining region Y)-boxes (SOX)","href":"/api/1.0/gene_family/SRY+%28sex+determining+region+Y%29-boxes+%28SOX%29"}]}