{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:728","gene_name":"ARVCF, delta catenin family member","omim_gene":["602269"],"alias_name":null,"gene_symbol":"ARVCF","hgnc_symbol":"ARVCF","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"22:19957419-20004331","ensembl_id":"ENSG00000099889"}},"GRch38":{"90":{"location":"22:19969896-20016808","ensembl_id":"ENSG00000099889"}}},"hgnc_date_symbol_changed":"1996-10-11"},"entity_type":"gene","entity_name":"ARVCF","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26887379"],"evidence":["Expert Review Red","Literature"],"phenotypes":["HSCR","Hirschsprung s Disease risk"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":63,"hash_id":"58c7f5008f620328d77ce70f","name":"Familial Hirschsprung Disease","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.6","version_created":"2019-06-20T15:11:10.292595Z","relevant_disorders":[],"stats":{"number_of_genes":62,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}