{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PZ"],"biotype":"protein_coding","hgnc_id":"HGNC:9460","gene_name":"protein Z, vitamin K dependent plasma glycoprotein","omim_gene":["176895"],"alias_name":null,"gene_symbol":"PROZ","hgnc_symbol":"PROZ","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"13:113812968-113826694","ensembl_id":"ENSG00000126231"}},"GRch38":{"90":{"location":"13:113158654-113172383","ensembl_id":"ENSG00000126231"}}},"hgnc_date_symbol_changed":"1999-06-03"},"entity_type":"gene","entity_name":"PROZ","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["15638861"],"evidence":["Other"],"phenotypes":["Protein Z deficiency","thromboembolic complication during pregnancy"],"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":["PZ"],"biotype":"protein_coding","hgnc_id":"HGNC:9460","gene_name":"protein Z, vitamin K dependent plasma glycoprotein","omim_gene":["176895"],"alias_name":null,"gene_symbol":"PROZ","hgnc_symbol":"PROZ","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"13:113812968-113826694","ensembl_id":"ENSG00000126231"}},"GRch38":{"90":{"location":"13:113158654-113172383","ensembl_id":"ENSG00000126231"}}},"hgnc_date_symbol_changed":"1999-06-03"},"entity_type":"gene","entity_name":"PROZ","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Wessex and West Midlands GLH","Expert Review Amber","NHS GMS","London South GLH"],"phenotypes":["614024 Protein Z deficiency"],"mode_of_inheritance":"BOTH monoallelic and biallelic, 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."}]}}]}