{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:2894","gene_name":"dickkopf WNT signaling pathway inhibitor 4","omim_gene":["605417"],"alias_name":null,"gene_symbol":"DKK4","hgnc_symbol":"DKK4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"8:42231586-42234750","ensembl_id":"ENSG00000104371"}},"GRch38":{"90":{"location":"8:42374068-42377232","ensembl_id":"ENSG00000104371"}}},"hgnc_date_symbol_changed":"2000-09-01"},"entity_type":"gene","entity_name":"DKK4","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["23936318","23108157"],"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"}]}}]}