{"symbol":"ABHD11","synonyms":["WBSCR21","PP1226"],"name":"abhydrolase domain containing 11","description":"This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Mar 2016]","ncbiEntrezGeneId":83451,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/83451","proteins":[{"symbol":"ABHDB_HUMAN","href":"/api/1.0/protein/ABHDB_HUMAN"}],"hgncRootFamilies":[{"name":"Abhydrolase domain containing (ABHD)","href":"/api/1.0/gene_family/Abhydrolase+domain+containing+%28ABHD%29"}]}