{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["NUP75","FLJ12549"],"biotype":"protein_coding","hgnc_id":"HGNC:8734","gene_name":"nucleoporin 85","omim_gene":["170285"],"alias_name":null,"gene_symbol":"NUP85","hgnc_symbol":"NUP85","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:73201754-73231853","ensembl_id":"ENSG00000125450"}},"GRch38":{"90":{"location":"17:75205659-75235758","ensembl_id":"ENSG00000125450"}}},"hgnc_date_symbol_changed":"2005-11-03"},"entity_type":"gene","entity_name":"NUP85","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["30179222"],"evidence":["Expert Review Green","NHS GMS"],"phenotypes":["Nephrotic syndrome, type 17 #618176"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":678,"hash_id":null,"name":"Unexplained paediatric onset end-stage renal disease","disease_group":"","disease_sub_group":"","status":"public","version":"0.43","version_created":"2019-09-25T12:25:36.245604Z","relevant_disorders":["R257"],"stats":{"number_of_genes":229,"number_of_strs":0,"number_of_regions":3},"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)"}]}},{"gene_data":{"alias":["NUP75","FLJ12549"],"biotype":"protein_coding","hgnc_id":"HGNC:8734","gene_name":"nucleoporin 85","omim_gene":["170285"],"alias_name":null,"gene_symbol":"NUP85","hgnc_symbol":"NUP85","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:73201754-73231853","ensembl_id":"ENSG00000125450"}},"GRch38":{"90":{"location":"17:75205659-75235758","ensembl_id":"ENSG00000125450"}}},"hgnc_date_symbol_changed":"2005-11-03"},"entity_type":"gene","entity_name":"NUP85","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["30179222"],"evidence":["Expert Review Green","NHS GMS"],"phenotypes":["Nephrotic syndrome, type 17 #618176"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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)"}]}}]}
