{"symbol":"GPD1L","synonyms":["GPD1-L"],"name":"glycerol-3-phosphate dehydrogenase 1-like","description":"The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS). [provided by RefSeq, Jul 2010]","ncbiEntrezGeneId":23171,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/23171","proteins":[{"symbol":"GPD1L_HUMAN","href":"/api/1.0/protein/GPD1L_HUMAN"}],"hgncRootFamilies":[]}