{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MOP1","HIF-1alpha","PASD8","HIF1","bHLHe78"],"biotype":"protein_coding","hgnc_id":"HGNC:4910","gene_name":"hypoxia inducible factor 1 alpha subunit","omim_gene":["603348"],"alias_name":null,"gene_symbol":"HIF1A","hgnc_symbol":"HIF1A","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"14:62162231-62214976","ensembl_id":"ENSG00000100644"}},"GRch38":{"90":{"location":"14:61695513-61748259","ensembl_id":"ENSG00000100644"}}},"hgnc_date_symbol_changed":"1995-03-27"},"entity_type":"gene","entity_name":"HIF1A","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["22274579"],"evidence":["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"}]}}]}