{"symbol":"FAM20A","synonyms":["AI1G","FP2747","AIGFS"],"name":"family with sequence similarity 20, member A","description":"This locus encodes a protein that is likely secreted and may function in hematopoiesis. A mutation at this locus has been associated with amelogenesis imperfecta and gingival hyperplasia syndrome. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Aug 2011]","ncbiEntrezGeneId":54757,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/54757","proteins":[{"symbol":"FA20A_HUMAN","href":"/api/1.0/protein/FA20A_HUMAN"}],"hgncRootFamilies":[]}