{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["OSP-L","CPETRL3"],"biotype":"protein_coding","hgnc_id":"HGNC:2033","gene_name":"claudin 10","omim_gene":["617579"],"alias_name":null,"gene_symbol":"CLDN10","hgnc_symbol":"CLDN10","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"13:96085858-96232013","ensembl_id":"ENSG00000134873"}},"GRch38":{"90":{"location":"13:95433604-95579759","ensembl_id":"ENSG00000134873"}}},"hgnc_date_symbol_changed":"1999-01-22"},"entity_type":"gene","entity_name":"CLDN10","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["19307729"],"evidence":["Expert Review Amber","NHS GMS"],"phenotypes":["Hypokalemic-alkalotic salt-losing tubulopathy (no OMIM number)","HELIX syndrome, 617671"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":292,"hash_id":"553f94d5bb5a1616e5ed45a4","name":"Renal tubulopathies","disease_group":"Renal and urinary tract disorders","disease_sub_group":"Disorders of function","status":"public","version":"1.193","version_created":"2019-10-09T09:34:39.432250Z","relevant_disorders":["Renal tubular acidosis","R198"],"stats":{"number_of_genes":55,"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)"}]}}]}