{"symbol":"TSPEAR","synonyms":["C21ORF29","TSP-EAR","DFNB98"],"name":"thrombospondin-type laminin G domain and EAR repeats","description":"This gene encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]","ncbiEntrezGeneId":54084,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/54084","proteins":[{"symbol":"TSEAR_HUMAN","href":"/api/1.0/protein/TSEAR_HUMAN"}],"hgncRootFamilies":[]}