{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:1806","gene_name":"caudal type homeobox 2","omim_gene":["600297"],"alias_name":null,"gene_symbol":"CDX2","hgnc_symbol":"CDX2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"13:28536274-28545276","ensembl_id":"ENSG00000165556"}},"GRch38":{"90":{"location":"13:27962137-27971139","ensembl_id":"ENSG00000165556"}}},"hgnc_date_symbol_changed":"1994-09-07"},"entity_type":"gene","entity_name":"CDX2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["19386267","27042391"],"evidence":["Expert Review Amber","Literature"],"phenotypes":["persistent cloaca"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":["watchlist"],"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"}]}}]}