{"symbol":"CUL7","synonyms":["3M1","CUL-7","KIAA0076","DJ20C7.5"],"name":"cullin 7","description":"The protein encoded by this gene is a component of an E3 ubiquitin-protein ligase complex. The encoded protein interacts with TP53, CUL9, and FBXW8 proteins. Defects in this gene are a cause of 3M syndrome type 1 (3M1). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]","ncbiEntrezGeneId":9820,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/9820","proteins":[{"symbol":"CUL7_HUMAN","href":"/api/1.0/protein/CUL7_HUMAN"}],"hgncRootFamilies":[]}