{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["SemE"],"biotype":"protein_coding","hgnc_id":"HGNC:10725","gene_name":"semaphorin 3C","omim_gene":["602645"],"alias_name":null,"gene_symbol":"SEMA3C","hgnc_symbol":"SEMA3C","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"7:80371854-80551675","ensembl_id":"ENSG00000075223"}},"GRch38":{"90":{"location":"7:80742538-80922359","ensembl_id":"ENSG00000075223"}}},"hgnc_date_symbol_changed":"1999-06-25"},"entity_type":"gene","entity_name":"SEMA3C","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["25839327"],"evidence":["Expert Review Amber","Alder Hey - Erasmus MC"],"phenotypes":["susceptibility to Hirschsprung disease"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":["watchlist"],"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"}]}}]}