{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MEGF2","HFMI1","FMI1","CDHF11","ADGRC3"],"biotype":"protein_coding","hgnc_id":"HGNC:3230","gene_name":"cadherin EGF LAG seven-pass G-type receptor 3","omim_gene":["604264"],"alias_name":["flamingo homolog 1 (Drosophila)","adhesion G protein-coupled receptor C3"],"gene_symbol":"CELSR3","hgnc_symbol":"CELSR3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"3:48673902-48700348","ensembl_id":"ENSG00000008300"}},"GRch38":{"90":{"location":"3:48636469-48662915","ensembl_id":"ENSG00000008300"}}},"hgnc_date_symbol_changed":"1998-03-25"},"entity_type":"gene","entity_name":"CELSR3","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27619161"],"evidence":["Expert Review Amber","Literature"],"phenotypes":["Hirschsprung disease"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","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"}]}}]}