{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:2041","gene_name":"claudin 2","omim_gene":["300520"],"alias_name":null,"gene_symbol":"CLDN2","hgnc_symbol":"CLDN2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"X:106143394-106174091","ensembl_id":"ENSG00000165376"}},"GRch38":{"90":{"location":"X:106900164-106930861","ensembl_id":"ENSG00000165376"}}},"hgnc_date_symbol_changed":"1998-11-19"},"entity_type":"gene","entity_name":"CLDN2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["29884332","29173301","28754779","26820620","26784911","26002935","25253127","23143602","28754779","24002981"],"evidence":["EUROPAC"],"phenotypes":[],"mode_of_inheritance":"","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."}]}}]}