{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CRL3","GLM-R","CRL","Glmr","IL-31RA"],"biotype":"protein_coding","hgnc_id":"HGNC:18969","gene_name":"interleukin 31 receptor A","omim_gene":["609510"],"alias_name":null,"gene_symbol":"IL31RA","hgnc_symbol":"IL31RA","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"5:55147207-55218678","ensembl_id":"ENSG00000164509"}},"GRch38":{"90":{"location":"5:55851379-55922853","ensembl_id":"ENSG00000164509"}}},"hgnc_date_symbol_changed":"2003-11-06"},"entity_type":"gene","entity_name":"IL31RA","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["19690585"],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["Amyloidosis, primary localized cutaneous, 2, 613955"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":60,"hash_id":"55a6566d22c1fc6710839b9c","name":"Periodic fever syndromes","disease_group":"Rheumatological disorders","disease_sub_group":"Multi-system inflammatory/autoimmune disorders","status":"public","version":"1.12","version_created":"2019-09-26T14:18:15.825616Z","relevant_disorders":["Periodic fever syndromes and amyloidosis"],"stats":{"number_of_genes":30,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["CRL3","GLM-R","CRL","Glmr","IL-31RA"],"biotype":"protein_coding","hgnc_id":"HGNC:18969","gene_name":"interleukin 31 receptor A","omim_gene":["609510"],"alias_name":null,"gene_symbol":"IL31RA","hgnc_symbol":"IL31RA","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"5:55147207-55218678","ensembl_id":"ENSG00000164509"}},"GRch38":{"90":{"location":"5:55851379-55922853","ensembl_id":"ENSG00000164509"}}},"hgnc_date_symbol_changed":"2003-11-06"},"entity_type":"gene","entity_name":"IL31RA","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber"],"phenotypes":[],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":559,"hash_id":null,"name":"Pigmentary skin disorders","disease_group":"","disease_sub_group":"","status":"public","version":"0.15","version_created":"2019-09-17T17:51:23.014209Z","relevant_disorders":[],"stats":{"number_of_genes":102,"number_of_strs":0,"number_of_regions":1},"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"}]}},{"gene_data":{"alias":["CRL3","GLM-R","CRL","Glmr","IL-31RA"],"biotype":"protein_coding","hgnc_id":"HGNC:18969","gene_name":"interleukin 31 receptor A","omim_gene":["609510"],"alias_name":null,"gene_symbol":"IL31RA","hgnc_symbol":"IL31RA","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"5:55147207-55218678","ensembl_id":"ENSG00000164509"}},"GRch38":{"90":{"location":"5:55851379-55922853","ensembl_id":"ENSG00000164509"}}},"hgnc_date_symbol_changed":"2003-11-06"},"entity_type":"gene","entity_name":"IL31RA","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","Expert Review Red","London North GLH"],"phenotypes":["?Amyloidosis, primary localized cutaneous 2, 613955"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","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."}]}}]}