{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["SM-20","PHD2","ZMYND6","HIFPH2"],"biotype":"protein_coding","hgnc_id":"HGNC:1232","gene_name":"egl-9 family hypoxia inducible factor 1","omim_gene":["606425"],"alias_name":["HIF prolyl hydroxylase 2"],"gene_symbol":"EGLN1","hgnc_symbol":"EGLN1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:231499497-231560790","ensembl_id":"ENSG00000135766"}},"GRch38":{"90":{"location":"1:231363751-231425044","ensembl_id":"ENSG00000135766"}}},"hgnc_date_symbol_changed":"2001-08-24"},"entity_type":"gene","entity_name":"EGLN1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27651169","27774468","23869443","19092153","16407130","17579185"],"evidence":["Expert Review Green","Illumina TruGenome Clinical Sequencing Services","Radboud University Medical Center, Nijmegen","Other"],"phenotypes":["Familial Erythrocytosis 609820","Polycythaemia","paraganglioma","phaeochromocytoma"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","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"}]}}]}