{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA0844","UAN"],"biotype":"protein_coding","hgnc_id":"HGNC:18194","gene_name":"zinc finger protein 365","omim_gene":["607818"],"alias_name":["Talanin"],"gene_symbol":"ZNF365","hgnc_symbol":"ZNF365","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"10:64133951-64431771","ensembl_id":"ENSG00000138311"}},"GRch38":{"90":{"location":"10:62374192-62672011","ensembl_id":"ENSG00000138311"}}},"hgnc_date_symbol_changed":"2003-06-13"},"entity_type":"gene","entity_name":"ZNF365","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Expert"],"phenotypes":["Possible cause of uric acid stones","{Nephrolithiasis, uric acid, susceptibility to}"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","tags":[],"panel":{"id":149,"hash_id":"553f94d5bb5a1616e5ed45a5","name":"Nephrocalcinosis or nephrolithiasis","disease_group":"Renal and urinary tract disorders","disease_sub_group":"Disorders of function","status":"public","version":"1.18","version_created":"2019-09-17T20:55:27.132282Z","relevant_disorders":["Renal tract calcification (or Nephrolithiasis or nephrocalcinosis)","Renal tract calcification (or Nephrolithiasis/nephrocalcinosis)","R256"],"stats":{"number_of_genes":42,"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)"}]}}]}