{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FPR","FMLP"],"biotype":"protein_coding","hgnc_id":"HGNC:3826","gene_name":"formyl peptide receptor 1","omim_gene":["136537"],"alias_name":null,"gene_symbol":"FPR1","hgnc_symbol":"FPR1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:52248425-52307363","ensembl_id":"ENSG00000171051"}},"GRch38":{"90":{"location":"19:51745172-51804110","ensembl_id":"ENSG00000171051"}}},"hgnc_date_symbol_changed":"1991-06-05"},"entity_type":"gene","entity_name":"FPR1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["10882119","20203610","8224916","2910576","28371599","29105764"],"evidence":["Expert Review Amber","IUIS Classification February 2018","Victorian Clinical Genetics Services","ESID Registry 20171117","GRID V2.0"],"phenotypes":["Periodontitis","Localized juvenile peridontitis","Periodontitis only","Congenital defects of phagocyte number or function"],"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."}]}}]}