{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA1278","FU"],"biotype":"protein_coding","hgnc_id":"HGNC:17209","gene_name":"serine/threonine kinase 36","omim_gene":["607652"],"alias_name":["fused homolog (Drosophila)"],"gene_symbol":"STK36","hgnc_symbol":"STK36","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"2:219536749-219567439","ensembl_id":"ENSG00000163482"}},"GRch38":{"90":{"location":"2:218672026-218702716","ensembl_id":"ENSG00000163482"}}},"hgnc_date_symbol_changed":"2001-11-22"},"entity_type":"gene","entity_name":"STK36","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["28543983"],"evidence":["Expert Review Amber","NHS GMS"],"phenotypes":[],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":550,"hash_id":null,"name":"Respiratory ciliopathies including non-CF bronchiectasis","disease_group":"","disease_sub_group":"","status":"public","version":"0.156","version_created":"2019-09-27T18:48:31.875976Z","relevant_disorders":["R189"],"stats":{"number_of_genes":61,"number_of_strs":0,"number_of_regions":0},"types":[{"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)"}]}}]}