{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["EP"],"biotype":"protein_coding","hgnc_id":"HGNC:3415","gene_name":"erythropoietin","omim_gene":["133170"],"alias_name":null,"gene_symbol":"EPO","hgnc_symbol":"EPO","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"7:100318423-100321323","ensembl_id":"ENSG00000130427"}},"GRch38":{"90":{"location":"7:100720800-100723700","ensembl_id":"ENSG00000130427"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"EPO","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27651169"],"evidence":["Expert Review Red","Literature"],"phenotypes":["Hereditary Erythrocytosis"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":157,"hash_id":"58c7fba38f6203345887d4f5","name":"Hereditary Erythrocytosis","disease_group":"","disease_sub_group":"","status":"public","version":"1.1","version_created":"2017-11-05T02:37:20.137591Z","relevant_disorders":[],"stats":{"number_of_genes":13,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["EP"],"biotype":"protein_coding","hgnc_id":"HGNC:3415","gene_name":"erythropoietin","omim_gene":["133170"],"alias_name":null,"gene_symbol":"EPO","hgnc_symbol":"EPO","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:100318423-100321323","ensembl_id":"ENSG00000130427"}},"GRch38":{"90":{"location":"7:100720800-100723700","ensembl_id":"ENSG00000130427"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"EPO","confidence_level":"1","penetrance":"unknown","mode_of_pathogenicity":null,"publications":["20655265","29514032","28283061"],"evidence":["Expert Review Red","Literature"],"phenotypes":["DBA","Diamond-Blackfan anemia-like (AR), 617911","Erythrocytosis, familial 5 (AD), 617907"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","tags":[],"panel":{"id":159,"hash_id":"58a70e858f62037e8779b2e8","name":"Cytopenias and congenital anaemias","disease_group":"Haematological disorders","disease_sub_group":"Anaemias and red cell disorders","status":"public","version":"1.73","version_created":"2019-09-23T11:25:32.403071Z","relevant_disorders":["Aplastic anaemia with or without paroxysmal nocturnal haemoglobinuria","Apparent aplastic anaemia or paroxysmal nocturnal haemoglobinuria","Congenital anaemias","Early onset pancytopenia and red cell disorders","Anaemias and red cell disorders","Cytopaenias and congenital anaemias","Cytopenia and pancytopenia"],"stats":{"number_of_genes":219,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}
