{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["hCAP-D3","CAP-D3","hHCP-6","KIAA0056","FLJ42888","hcp-6"],"biotype":"protein_coding","hgnc_id":"HGNC:28952","gene_name":"non-SMC condensin II complex subunit D3","omim_gene":["609276"],"alias_name":null,"gene_symbol":"NCAPD3","hgnc_symbol":"NCAPD3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"11:134020014-134095348","ensembl_id":"ENSG00000151503"}},"GRch38":{"90":{"location":"11:134150119-134225454","ensembl_id":"ENSG00000151503"}}},"hgnc_date_symbol_changed":"2006-09-04"},"entity_type":"gene","entity_name":"NCAPD3","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["27737959"],"evidence":["DD-Gene2Phenotype","Expert Review Red"],"phenotypes":["Microcephaly with short stature"],"mode_of_inheritance":"","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}