{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:35123","gene_name":"forkhead box I3","omim_gene":["612351"],"alias_name":null,"gene_symbol":"FOXI3","hgnc_symbol":"FOXI3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"2:88747726-88752131","ensembl_id":"ENSG00000214336"}},"GRch38":{"90":{"location":"2:88446787-88452656","ensembl_id":"ENSG00000214336"}}},"hgnc_date_symbol_changed":"2008-12-18"},"entity_type":"gene","entity_name":"FOXI3","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Literature","Expert Review Red","Expert list"],"phenotypes":["Bilateral Microtia","Congenital aural atresia"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":251,"hash_id":"57f4dbd18f62036d37cfe4e4","name":"Deafness and congenital structural abnormalities","disease_group":"Hearing and ear disorders","disease_sub_group":"Deafness and congenital structural abnormalities","status":"public","version":"1.17","version_created":"2019-06-20T15:10:56.166309Z","relevant_disorders":["Bilateral microtia","Ear malformations with hearing impairment","Ear malformations","Familial hemifacial microsomia"],"stats":{"number_of_genes":54,"number_of_strs":0,"number_of_regions":3},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}