{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:14544","gene_name":"WNK lysine deficient protein kinase 4","omim_gene":["601844"],"alias_name":null,"gene_symbol":"WNK4","hgnc_symbol":"WNK4","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"17:40932696-40948954","ensembl_id":"ENSG00000126562"}},"GRch38":{"90":{"location":"17:42780678-42796936","ensembl_id":"ENSG00000126562"}}},"hgnc_date_symbol_changed":"2005-01-19"},"entity_type":"gene","entity_name":"WNK4","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["12107233","12515852","11498583"],"evidence":["Expert Review Green","Radboud University Medical Center, Nijmegen","UKGTN","Illumina TruGenome Clinical Sequencing Services","Expert list"],"phenotypes":["Pseudohypoaldosteronism, type IIB, 614491"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":314,"hash_id":"553f9697bb5a1616e5ed45d4","name":"Extreme early-onset hypertension","disease_group":"Renal and urinary tract disorders","disease_sub_group":"Disorders of function","status":"public","version":"1.10","version_created":"2018-12-16T17:33:34.572280Z","relevant_disorders":[],"stats":{"number_of_genes":25,"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 Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."}]}},{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:14544","gene_name":"WNK lysine deficient protein kinase 4","omim_gene":["601844"],"alias_name":null,"gene_symbol":"WNK4","hgnc_symbol":"WNK4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:40932696-40948954","ensembl_id":"ENSG00000126562"}},"GRch38":{"90":{"location":"17:42780678-42796936","ensembl_id":"ENSG00000126562"}}},"hgnc_date_symbol_changed":"2005-01-19"},"entity_type":"gene","entity_name":"WNK4","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["11498583"],"evidence":["Expert Review Green","NHS GMS"],"phenotypes":["Pseudohypoaldosteronism, type IIB, 614491"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","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)"}]}}]}