{"symbol":"TMEM126A","synonyms":["OPA7"],"name":"transmembrane protein 126A","description":"The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]","ncbiEntrezGeneId":84233,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/84233","proteins":[{"symbol":"T126A_HUMAN","href":"/api/1.0/protein/T126A_HUMAN"}],"hgncRootFamilies":[]}