{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["AF6q21","FOXO2"],"biotype":"protein_coding","hgnc_id":"HGNC:3821","gene_name":"forkhead box O3","omim_gene":["602681"],"alias_name":null,"gene_symbol":"FOXO3","hgnc_symbol":"FOXO3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"6:108881038-109005977","ensembl_id":"ENSG00000118689"}},"GRch38":{"90":{"location":"6:108559835-108684774","ensembl_id":"ENSG00000118689"}}},"hgnc_date_symbol_changed":"2007-05-02"},"entity_type":"gene","entity_name":"FOXO3","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["25208626"],"evidence":["Literature"],"phenotypes":["Hamartomatous polyposis syndromes including Peutz-Jeghers and PTEN hamartoma tumor syndromes"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":254,"hash_id":"591444928f620348d4b20c16","name":"GI tract tumours","disease_group":"Tumour syndromes","disease_sub_group":"GI tract","status":"public","version":"1.18","version_created":"2019-08-05T14:17:21.117330Z","relevant_disorders":["GI tract tumours","Familial colon cancer","Multiple bowel polyps","Peutz-Jeghers syndrome","GI tract","Inherited colorectal cancer (with or without polyposis)"],"stats":{"number_of_genes":30,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}