{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["Lp(a)"],"biotype":"protein_coding","hgnc_id":"HGNC:6667","gene_name":"lipoprotein(a)","omim_gene":["152200"],"alias_name":["apolipoprotein(a)"],"gene_symbol":"LPA","hgnc_symbol":"LPA","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"6:160952515-161087407","ensembl_id":"ENSG00000198670"}},"GRch38":{"90":{"location":"6:160531483-160664259","ensembl_id":"ENSG00000198670"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"LPA","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["11698280","9164807"],"evidence":["Other"],"phenotypes":["thromboembolism","elevated serum Lp(a) levels","childhood thrombosis associated with raised Lp(a) levels"],"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"}]}}]}