{"symbol":"MECR","synonyms":["FASN2B","DYTOABG","CGI-63","NRBF1","ETR1"],"name":"mitochondrial trans-2-enoyl-CoA reductase","description":"The protein encoded by this gene is an oxidoreductase that catalyzes the last step in mitochondrial fatty acid synthesis. Defects in this gene are a cause of childhood-onset dystonia and optic atrophy. [provided by RefSeq, Mar 2017]","ncbiEntrezGeneId":51102,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/51102","proteins":[{"symbol":"MECR_HUMAN","href":"/api/1.0/protein/MECR_HUMAN"}],"hgncRootFamilies":[]}