{"count":5,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CSIF","TGIF","IL10A","IL-10"],"biotype":"protein_coding","hgnc_id":"HGNC:5962","gene_name":"interleukin 10","omim_gene":["124092"],"alias_name":["cytokine synthesis inhibitory factor","T-cell growth inhibitory factor"],"gene_symbol":"IL10","hgnc_symbol":"IL10","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:206940947-206945839","ensembl_id":"ENSG00000136634"}},"GRch38":{"90":{"location":"1:206767602-206772494","ensembl_id":"ENSG00000136634"}}},"hgnc_date_symbol_changed":"1991-10-31"},"entity_type":"gene","entity_name":"IL10","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27302973"],"evidence":["Expert Review Amber","UKGTN","Eligibility statement prior genetic testing","Expert list"],"phenotypes":["IL-10 signalling defects / deficiency","IL10-Related Inflammatory Bowel Disease"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":176,"hash_id":"56ba026c22c1fc5025762b50","name":"Infantile enterocolitis & monogenic inflammatory bowel disease","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.16","version_created":"2017-11-05T02:37:20.171671Z","relevant_disorders":["Infantile enterocolitis and monogenic inflammatory bowel disease"],"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":["CSIF","TGIF","IL10A","IL-10"],"biotype":"protein_coding","hgnc_id":"HGNC:5962","gene_name":"interleukin 10","omim_gene":["124092"],"alias_name":["cytokine synthesis inhibitory factor","T-cell growth inhibitory factor"],"gene_symbol":"IL10","hgnc_symbol":"IL10","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:206940947-206945839","ensembl_id":"ENSG00000136634"}},"GRch38":{"90":{"location":"1:206767602-206772494","ensembl_id":"ENSG00000136634"}}},"hgnc_date_symbol_changed":"1991-10-31"},"entity_type":"gene","entity_name":"IL10","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["28787010"],"evidence":["Literature"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":394,"hash_id":null,"name":"Familial Meniere Disease","disease_group":"Hearing and ear disorders","disease_sub_group":"Other hearing and ear disorders","status":"public","version":"1.1","version_created":"2018-01-17T16:26:29.432517Z","relevant_disorders":[],"stats":{"number_of_genes":130,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["CSIF","TGIF","IL10A","IL-10"],"biotype":"protein_coding","hgnc_id":"HGNC:5962","gene_name":"interleukin 10","omim_gene":["124092"],"alias_name":["cytokine synthesis inhibitory factor","T-cell growth inhibitory factor"],"gene_symbol":"IL10","hgnc_symbol":"IL10","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:206940947-206945839","ensembl_id":"ENSG00000136634"}},"GRch38":{"90":{"location":"1:206767602-206772494","ensembl_id":"ENSG00000136634"}}},"hgnc_date_symbol_changed":"1991-10-31"},"entity_type":"gene","entity_name":"IL10","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":[],"evidence":["Expert Review Green","Other","UKGTN"],"phenotypes":["Inflammatory Bowel Disease (Very Early Onset)","Crohn disease"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":33,"hash_id":"56ba026422c1fc5025762b4f","name":"Gastrointestinal epithelial barrier disorders","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.59","version_created":"2019-06-20T15:11:44.535737Z","relevant_disorders":[],"stats":{"number_of_genes":82,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["CSIF","TGIF","IL10A","IL-10"],"biotype":"protein_coding","hgnc_id":"HGNC:5962","gene_name":"interleukin 10","omim_gene":["124092"],"alias_name":["cytokine synthesis inhibitory factor","T-cell growth inhibitory factor"],"gene_symbol":"IL10","hgnc_symbol":"IL10","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:206940947-206945839","ensembl_id":"ENSG00000136634"}},"GRch38":{"90":{"location":"1:206767602-206772494","ensembl_id":"ENSG00000136634"}}},"hgnc_date_symbol_changed":"1991-10-31"},"entity_type":"gene","entity_name":"IL10","confidence_level":"0","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Removed","Literature"],"phenotypes":[],"mode_of_inheritance":"Unknown","tags":["promoter"],"panel":{"id":45,"hash_id":"5763f6508f620350a1996055","name":"Sudden death in young people","disease_group":"Cardiovascular disorders","disease_sub_group":"Cardiac arrhythmia","status":"public","version":"1.12","version_created":"2019-06-20T15:15:17.414434Z","relevant_disorders":["Unexplained sudden death in the young"],"stats":{"number_of_genes":35,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["CSIF","TGIF","IL10A","IL-10"],"biotype":"protein_coding","hgnc_id":"HGNC:5962","gene_name":"interleukin 10","omim_gene":["124092"],"alias_name":["cytokine synthesis inhibitory factor","T-cell growth inhibitory factor"],"gene_symbol":"IL10","hgnc_symbol":"IL10","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:206940947-206945839","ensembl_id":"ENSG00000136634"}},"GRch38":{"90":{"location":"1:206767602-206772494","ensembl_id":"ENSG00000136634"}}},"hgnc_date_symbol_changed":"1991-10-31"},"entity_type":"gene","entity_name":"IL10","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["19890111","20951137"],"evidence":["NHS GMS","North West GLH","London North GLH","Expert Review Green","IUIS Classification February 2018","Victorian Clinical Genetics Services","ESID Registry 20171117","GRID V2.0","GOSH PID v.8.0"],"phenotypes":["Early-onset inflammatory bowel disease","Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome","Inflammatory bowel disease (IBD) Folliculitis, recurrent respiratory diseases, arthritis,","Diseases of Immune Dysregulation"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":398,"hash_id":null,"name":"Primary immunodeficiency","disease_group":"","disease_sub_group":"","status":"public","version":"1.132","version_created":"2019-09-27T14:37:49.085568Z","relevant_disorders":["Primary immunodeficiency disorders","A- or hypo-gammaglobulinaemia","Congenital neutropaenia","Agranulocytosis","Combined B and T cell defect","Inherited complement deficiency","SCID","Primary immune disorder","Primary immunodeficiency","A-gammaglobulinaemia","Agammaglobulinaemia","hypo-gammaglobulinaemia","hypogammaglobulinemia","immune deficiency syndromes","Severe combined immunodeficiency","Congenital neutopenia","Familial haemophagocytic lymphohistiocytic disorders","Familial hemophagocytic lymphohistiocytic disorders","PID","Sepsis","Disseminated non-tuberculous mycobacterial infection","R15"],"stats":{"number_of_genes":395,"number_of_strs":0,"number_of_regions":2},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."}]}}]}
