{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["p24"],"biotype":"protein_coding","hgnc_id":"HGNC:17881","gene_name":"neurensin 1","omim_gene":["616630"],"alias_name":null,"gene_symbol":"NRSN1","hgnc_symbol":"NRSN1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"6:24126350-24155128","ensembl_id":"ENSG00000152954"}},"GRch38":{"90":{"location":"6:24126122-24154900","ensembl_id":"ENSG00000152954"}}},"hgnc_date_symbol_changed":"2006-07-04"},"entity_type":"gene","entity_name":"NRSN1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["22325380"],"evidence":["Expert Review Red","Literature"],"phenotypes":["Hirschsprung disease","HD"],"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"}]}}]}