{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FBP17","KIAA0554"],"biotype":"protein_coding","hgnc_id":"HGNC:17069","gene_name":"formin binding protein 1","omim_gene":["606191"],"alias_name":null,"gene_symbol":"FNBP1","hgnc_symbol":"FNBP1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"9:132649466-132805473","ensembl_id":"ENSG00000187239"}},"GRch38":{"90":{"location":"9:129887187-130043194","ensembl_id":"ENSG00000187239"}}},"hgnc_date_symbol_changed":"2002-11-25"},"entity_type":"gene","entity_name":"FNBP1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["23936318"],"evidence":["Literature"],"phenotypes":["anorectal malformation"],"mode_of_inheritance":"","tags":[],"panel":{"id":253,"hash_id":"576cd7e38f62036097d6cc9c","name":"Non-syndromic familial congenital anorectal malformations","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.5","version_created":"2019-06-20T15:15:14.416374Z","relevant_disorders":[],"stats":{"number_of_genes":51,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}