{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["BK"],"biotype":"protein_coding","hgnc_id":"HGNC:6383","gene_name":"kininogen 1","omim_gene":["612358"],"alias_name":["alpha-2-thiol proteinase inhibitor","bradykinin"],"gene_symbol":"KNG1","hgnc_symbol":"KNG1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"3:186435065-186461743","ensembl_id":"ENSG00000113889"}},"GRch38":{"90":{"location":"3:186717276-186743954","ensembl_id":"ENSG00000113889"}}},"hgnc_date_symbol_changed":"2004-05-26"},"entity_type":"gene","entity_name":"KNG1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["7901207","28445521","28053049"],"evidence":["Expert Review Green","BRIDGE Study Tier 1 Gene"],"phenotypes":["Coagulaton disorder","High Molecular Weight Kininogen Deficiency"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":175,"hash_id":"5763f32a8f620350a22bccde","name":"Inherited bleeding disorders","disease_group":"Haematological and immunological disorders","disease_sub_group":"Haemostasis disorders","status":"public","version":"1.156","version_created":"2019-08-09T13:55:23.938344Z","relevant_disorders":["Inherited platelet disorders","Monogenic thrombophilia","Inherited bleeding and or platelet disorders","Unprovoked Thrombosis before 40","Monogenic venous thrombosis"],"stats":{"number_of_genes":119,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["BK"],"biotype":"protein_coding","hgnc_id":"HGNC:6383","gene_name":"kininogen 1","omim_gene":["612358"],"alias_name":["alpha-2-thiol proteinase inhibitor","bradykinin"],"gene_symbol":"KNG1","hgnc_symbol":"KNG1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:186435065-186461743","ensembl_id":"ENSG00000113889"}},"GRch38":{"90":{"location":"3:186717276-186743954","ensembl_id":"ENSG00000113889"}}},"hgnc_date_symbol_changed":"2004-05-26"},"entity_type":"gene","entity_name":"KNG1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["12576314","24492696","7901207"],"evidence":["North West GLH","Yorkshire and North East GLH","London South GLH","NHS GMS","Expert Review Green","Wessex and West Midlands GLH"],"phenotypes":["228960 [High molecular weight kininogen deficiency]","228960 [High molecular weight kininogen deficiency]/[Kininogen deficiency]","[Kininogen deficiency]"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":545,"hash_id":null,"name":"Bleeding and platelet disorders","disease_group":"","disease_sub_group":"","status":"public","version":"0.78","version_created":"2019-09-23T11:07:54.788299Z","relevant_disorders":["R90"],"stats":{"number_of_genes":111,"number_of_strs":0,"number_of_regions":0},"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)"}]}}]}