{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:3416","gene_name":"erythropoietin receptor","omim_gene":["133171"],"alias_name":null,"gene_symbol":"EPOR","hgnc_symbol":"EPOR","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"19:11488236-11495018","ensembl_id":"ENSG00000187266"}},"GRch38":{"90":{"location":"19:11377205-11384342","ensembl_id":"ENSG00000187266"}}},"hgnc_date_symbol_changed":"1990-05-14"},"entity_type":"gene","entity_name":"EPOR","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27774468","23859443","18492694","8506290","11929803"],"evidence":["Expert Review Green","Illumina TruGenome Clinical Sequencing Services","Other"],"phenotypes":["Polcythaemia","erythrocytosis","Familial Erythrocytosis"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status 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"}]}}]}