{"symbol":"SERAC1","synonyms":[],"name":"serine active site containing 1","description":"The protein encoded by this gene is a phosphatidylglycerol remodeling protein found at the interface of mitochondria and endoplasmic reticula, where it mediates phospholipid exchange. The encoded protein plays a major role in mitochondrial function and intracellular cholesterol trafficking. Defects in this gene are a cause of 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome (MEGDEL). Two transcript variants, one protein-coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Aug 2012]","ncbiEntrezGeneId":84947,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/84947","proteins":[{"symbol":"SRAC1_HUMAN","href":"/api/1.0/protein/SRAC1_HUMAN"}],"hgncRootFamilies":[]}