{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA0197","FLJ22583"],"biotype":"protein_coding","hgnc_id":"HGNC:18017","gene_name":"nucleoporin 160","omim_gene":["607614"],"alias_name":null,"gene_symbol":"NUP160","hgnc_symbol":"NUP160","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"11:47799639-47870107","ensembl_id":"ENSG00000030066"}},"GRch38":{"90":{"location":"11:47778087-47848555","ensembl_id":"ENSG00000030066"}}},"hgnc_date_symbol_changed":"2002-01-18"},"entity_type":"gene","entity_name":"NUP160","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["30179222"],"evidence":["NHS GMS"],"phenotypes":["?Nephrotic syndrome, type 19 #618178"],"mode_of_inheritance":"","tags":[],"panel":{"id":106,"hash_id":"55af787822c1fc78a829f89f","name":"Proteinuric renal disease","disease_group":"Renal and urinary tract disorders","disease_sub_group":"Syndromes with prominent renal abnormalities","status":"public","version":"1.225","version_created":"2019-10-09T10:57:45.692187Z","relevant_disorders":["R195"],"stats":{"number_of_genes":95,"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)"}]}}]}