{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CLCR","ELA4"],"biotype":"protein_coding","hgnc_id":"HGNC:2523","gene_name":"chymotrypsin C","omim_gene":["601405"],"alias_name":["elastase 4","caldecrin"],"gene_symbol":"CTRC","hgnc_symbol":"CTRC","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:15764935-15775737","ensembl_id":"ENSG00000162438"}},"GRch38":{"90":{"location":"1:15438439-15449242","ensembl_id":"ENSG00000162438"}}},"hgnc_date_symbol_changed":"2000-06-08"},"entity_type":"gene","entity_name":"CTRC","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["18059268","18172691","28502372"],"evidence":["NHS GMS","Expert Review Amber","EUROPAC"],"phenotypes":["{Pancreatitis, chronic, susceptibility to} 167800"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":386,"hash_id":null,"name":"Pancreatitis","disease_group":"","disease_sub_group":"","status":"public","version":"2.0","version_created":"2019-09-04T09:45:14.660178Z","relevant_disorders":["R175"],"stats":{"number_of_genes":16,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}