{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["REL-B"],"biotype":"protein_coding","hgnc_id":"HGNC:9956","gene_name":"RELB proto-oncogene, NF-kB subunit","omim_gene":["604758"],"alias_name":null,"gene_symbol":"RELB","hgnc_symbol":"RELB","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:45504688-45541452","ensembl_id":"ENSG00000104856"}},"GRch38":{"90":{"location":"19:45001430-45038198","ensembl_id":"ENSG00000104856"}}},"hgnc_date_symbol_changed":"1995-10-02"},"entity_type":"gene","entity_name":"RELB","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["26385063"],"evidence":["IUIS Classification February 2018","Expert Review Red","Combined B and T cell defect v1.12"],"phenotypes":["?Immunodeficiency 53, 617585","Recurrent infections","Immunodeficiencies affecting cellular and humoral immunity"],"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."}]}}]}