{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PSP"],"biotype":"protein_coding","hgnc_id":"HGNC:9579","gene_name":"persephin","omim_gene":["602921"],"alias_name":null,"gene_symbol":"PSPN","hgnc_symbol":"PSPN","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"19:6375159-6379069","ensembl_id":"ENSG00000125650"}},"GRch38":{"90":{"location":"19:6375148-6379058","ensembl_id":"ENSG00000125650"}}},"hgnc_date_symbol_changed":"1997-10-10"},"entity_type":"gene","entity_name":"PSPN","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["28543993","21206993","18970938"],"evidence":["Expert Review Red","Alder Hey - Erasmus MC"],"phenotypes":["susceptibility to Hirschsprung disease"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","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"}]}}]}