{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["TNF-R","TNFAR","TNFR60","TNF-R-I","CD120a","TNF-R55"],"biotype":"protein_coding","hgnc_id":"HGNC:11916","gene_name":"TNF receptor superfamily member 1A","omim_gene":["191190"],"alias_name":null,"gene_symbol":"TNFRSF1A","hgnc_symbol":"TNFRSF1A","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"12:6437923-6451280","ensembl_id":"ENSG00000067182"}},"GRch38":{"90":{"location":"12:6328757-6342114","ensembl_id":"ENSG00000067182"}}},"hgnc_date_symbol_changed":"1991-01-15"},"entity_type":"gene","entity_name":"TNFRSF1A","confidence_level":"3","penetrance":"Incomplete","mode_of_pathogenicity":"","publications":["10199409"],"evidence":["Expert Review Green","Eligibility statement prior genetic testing","Emory Genetics Laboratory"],"phenotypes":["Hereditary Periodic Fever Syndromes","Periodic fever, familial, 142680"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT 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(TRAPS)","Recurrent fever, serositis, rash, and ocular or joint inflammation","Autoinflammatory Disorders"],"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 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