{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PHD1","HIFPH1"],"biotype":"protein_coding","hgnc_id":"HGNC:14660","gene_name":"egl-9 family hypoxia inducible factor 2","omim_gene":["606424"],"alias_name":["HIF prolyl hydroxylase 1"],"gene_symbol":"EGLN2","hgnc_symbol":"EGLN2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"19:41304901-41314338","ensembl_id":"ENSG00000269858"}},"GRch38":{"90":{"location":"19:40798996-40808433","ensembl_id":"ENSG00000269858"}}},"hgnc_date_symbol_changed":"2001-08-21"},"entity_type":"gene","entity_name":"EGLN2","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["22274579"],"evidence":["Expert Review Red","Literature"],"phenotypes":["Familial 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"}]}}]}