{"symbol":"GSDME","synonyms":[],"name":"gasdermin E","description":"Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]","ncbiEntrezGeneId":1687,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gove/gene/1687","proteins":[],"hgncRootFamilies":[]}