{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:2296","gene_name":"carboxypeptidase A1","omim_gene":["114850"],"alias_name":["pancreatic carboxypeptidase A"],"gene_symbol":"CPA1","hgnc_symbol":"CPA1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:130020180-130027955","ensembl_id":"ENSG00000091704"}},"GRch38":{"90":{"location":"7:130380339-130388114","ensembl_id":"ENSG00000091704"}}},"hgnc_date_symbol_changed":"1986-01-01"},"entity_type":"gene","entity_name":"CPA1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["23955596","28497564","28258133","28650851"],"evidence":["NHS GMS","Expert Review Amber","EUROPAC"],"phenotypes":["Chronic pancreatitis","Hereditary chronic pancreatitis"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":["watchlist"],"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."}]}}]}