{"symbol":"DNAJC30","synonyms":["WBSCR18"],"name":"DnaJ (Hsp40) homolog, subfamily C, member 30","description":"This intronless gene encodes a member of the DNAJ molecular chaperone homology domain-containing protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Jul 2008]","ncbiEntrezGeneId":84277,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/84277","proteins":[{"symbol":"DJC30_HUMAN","href":"/api/1.0/protein/DJC30_HUMAN"}],"hgncRootFamilies":[{"name":"Heat shock proteins","href":"/api/1.0/gene_family/Heat+shock+proteins"}]}