{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:11608","gene_name":"thromboxane A2 receptor","omim_gene":["188070"],"alias_name":null,"gene_symbol":"TBXA2R","hgnc_symbol":"TBXA2R","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"19:3594504-3606838","ensembl_id":"ENSG00000006638"}},"GRch38":{"90":{"location":"19:3594506-3606840","ensembl_id":"ENSG00000006638"}}},"hgnc_date_symbol_changed":"1991-08-08"},"entity_type":"gene","entity_name":"TBXA2R","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Green","BRIDGE Study Tier 1 Gene"],"phenotypes":["Thromboxane A2 receptor defect"],"mode_of_inheritance":"BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), 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:11608","gene_name":"thromboxane A2 receptor","omim_gene":["188070"],"alias_name":null,"gene_symbol":"TBXA2R","hgnc_symbol":"TBXA2R","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:3594504-3606838","ensembl_id":"ENSG00000006638"}},"GRch38":{"90":{"location":"19:3594506-3606840","ensembl_id":"ENSG00000006638"}}},"hgnc_date_symbol_changed":"1991-08-08"},"entity_type":"gene","entity_name":"TBXA2R","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["22517902","8972034","24452735","30089223","19828703","8428006"],"evidence":["North West GLH","Yorkshire and North East GLH","London South GLH","NHS GMS","Expert Review Green","Wessex and West Midlands GLH"],"phenotypes":["614009.BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO","BDPLT13","614009 BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO"],"mode_of_inheritance":"BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), 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)"}]}}]}