{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["IL-11","AGIF"],"biotype":"protein_coding","hgnc_id":"HGNC:5966","gene_name":"interleukin 11","omim_gene":["147681"],"alias_name":["adipogenesis inhibitory factor","oprelvekin"],"gene_symbol":"IL11","hgnc_symbol":"IL11","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"19:55875757-55881831","ensembl_id":"ENSG00000095752"}},"GRch38":{"90":{"location":"19:55364389-55370463","ensembl_id":"ENSG00000095752"}}},"hgnc_date_symbol_changed":"1991-08-06"},"entity_type":"gene","entity_name":"IL11","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26172388","28543993"],"evidence":["Expert Review Red","Literature"],"phenotypes":["risk of HSCR"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":63,"hash_id":"58c7f5008f620328d77ce70f","name":"Familial Hirschsprung Disease","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.6","version_created":"2019-06-20T15:11:10.292595Z","relevant_disorders":[],"stats":{"number_of_genes":62,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["IL-11","AGIF"],"biotype":"protein_coding","hgnc_id":"HGNC:5966","gene_name":"interleukin 11","omim_gene":["147681"],"alias_name":["adipogenesis inhibitory factor","oprelvekin"],"gene_symbol":"IL11","hgnc_symbol":"IL11","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:55875757-55881831","ensembl_id":"ENSG00000095752"}},"GRch38":{"90":{"location":"19:55364389-55370463","ensembl_id":"ENSG00000095752"}}},"hgnc_date_symbol_changed":"1991-08-06"},"entity_type":"gene","entity_name":"IL11","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"Other - please provide details in the comments","publications":["21741611"],"evidence":["DD-Gene2Phenotype","Expert Review Red"],"phenotypes":["CRANIOSYNOSTOSIS AND DENTAL ANOMALIES 614188"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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"}]}}]}