{"symbol":"FAM136A","synonyms":[],"name":"family with sequence similarity 136, member A","description":"This gene encodes a mitochondrially localized protein that is highly conserved across species. The gene is expressed in a variety of tissues including human lymphoblast cells and rat neurosensorial epithelium of the cristaampullaris. A mutation in this gene has been associated with familial Meniere\u0027s disease, a chronic disorder of the inner ear. Several pseudogenes of this gene are found on other chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]","ncbiEntrezGeneId":84908,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/84908","proteins":[{"symbol":"F136A_HUMAN","href":"/api/1.0/protein/F136A_HUMAN"}],"hgncRootFamilies":[]}