{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:7999","gene_name":"neuregulin 3","omim_gene":["605533"],"alias_name":null,"gene_symbol":"NRG3","hgnc_symbol":"NRG3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"10:83635070-84746935","ensembl_id":"ENSG00000185737"}},"GRch38":{"90":{"location":"10:81875314-82987179","ensembl_id":"ENSG00000185737"}}},"hgnc_date_symbol_changed":"1999-03-19"},"entity_type":"gene","entity_name":"NRG3","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27889765","22589734","23315268"],"evidence":["Expert Review Amber","Alder Hey - Erasmus MC"],"phenotypes":["susceptibility to Hirschsprung disease"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":["cnv"],"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"}]}}]}