{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["EPCR","CCD41","CD201"],"biotype":"protein_coding","hgnc_id":"HGNC:9452","gene_name":"protein C receptor","omim_gene":["600646"],"alias_name":null,"gene_symbol":"PROCR","hgnc_symbol":"PROCR","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"20:33759876-33765165","ensembl_id":"ENSG00000101000"}},"GRch38":{"90":{"location":"20:35172073-35216240","ensembl_id":"ENSG00000101000"}}},"hgnc_date_symbol_changed":"2000-06-26"},"entity_type":"gene","entity_name":"PROCR","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Other"],"phenotypes":["thrombosis"],"mode_of_inheritance":"","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":["EPCR","CCD41","CD201"],"biotype":"protein_coding","hgnc_id":"HGNC:9452","gene_name":"protein C receptor","omim_gene":["600646"],"alias_name":null,"gene_symbol":"PROCR","hgnc_symbol":"PROCR","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"20:33759876-33765165","ensembl_id":"ENSG00000101000"}},"GRch38":{"90":{"location":"20:35172073-35216240","ensembl_id":"ENSG00000101000"}}},"hgnc_date_symbol_changed":"2000-06-26"},"entity_type":"gene","entity_name":"PROCR","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Wessex and West Midlands GLH","North West GLH","Yorkshire and North East GLH","Expert Review Amber","NHS GMS","London South GLH"],"phenotypes":["?Thrombophilia"],"mode_of_inheritance":"BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","tags":[],"panel":{"id":516,"hash_id":null,"name":"Thrombophilia","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-09-23T14:53:24.252789Z","relevant_disorders":["R97"],"stats":{"number_of_genes":20,"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)"},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}