{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FCRN","alpha-chain"],"biotype":"protein_coding","hgnc_id":"HGNC:3621","gene_name":"Fc fragment of IgG receptor and transporter","omim_gene":["601437"],"alias_name":["heavy chain of the major histocompatibility complex class I-like Fc receptor","transmembrane alpha chain of the neonatal receptor"],"gene_symbol":"FCGRT","hgnc_symbol":"FCGRT","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:50010073-50029590","ensembl_id":"ENSG00000104870"}},"GRch38":{"90":{"location":"19:49506816-49526333","ensembl_id":"ENSG00000104870"}}},"hgnc_date_symbol_changed":"1995-08-23"},"entity_type":"gene","entity_name":"FCGRT","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":[],"evidence":["Expert Review Red","ESID Registry 20171117"],"phenotypes":["Fc receptor deficiencies"],"mode_of_inheritance":"","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."}]}}]}