{"count":4,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:3530","gene_name":"coagulation factor XII","omim_gene":["610619"],"alias_name":null,"gene_symbol":"F12","hgnc_symbol":"F12","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"5:176829141-176836577","ensembl_id":"ENSG00000131187"}},"GRch38":{"90":{"location":"5:177402140-177409576","ensembl_id":"ENSG00000131187"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"F12","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["2882793"],"evidence":["Expert Review Green","BRIDGE Study Tier 1 Gene"],"phenotypes":["Coagulaton disorder","Angioedema, hereditary, type 3 (AD)","Angioedema, hereditary, type III","Factor 12 deficiency (AR)","Factor XII deficiency"],"mode_of_inheritance":"BOTH monoallelic and 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":[],"biotype":"protein_coding","hgnc_id":"HGNC:3530","gene_name":"coagulation factor XII","omim_gene":["610619"],"alias_name":null,"gene_symbol":"F12","hgnc_symbol":"F12","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"5:176829141-176836577","ensembl_id":"ENSG00000131187"}},"GRch38":{"90":{"location":"5:177402140-177409576","ensembl_id":"ENSG00000131187"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"F12","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - 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