{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FREAC2"],"biotype":"protein_coding","hgnc_id":"HGNC:3810","gene_name":"forkhead box F2","omim_gene":["603250"],"alias_name":null,"gene_symbol":"FOXF2","hgnc_symbol":"FOXF2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:1390069-1395832","ensembl_id":"ENSG00000137273"}},"GRch38":{"90":{"location":"6:1389834-1395597","ensembl_id":"ENSG00000137273"}}},"hgnc_date_symbol_changed":"1995-06-05"},"entity_type":"gene","entity_name":"FOXF2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["27068588"],"evidence":["Literature"],"phenotypes":["Small vessel stroke"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":50,"hash_id":"5693787622c1fc25158f3c9a","name":"Familial cerebral small vessel disease","disease_group":"Cardiovascular disorders","disease_sub_group":"Arteriopathies","status":"public","version":"1.6","version_created":"2019-01-20T15:15:42.512731Z","relevant_disorders":[],"stats":{"number_of_genes":16,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."}]}}]}