{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:8075","gene_name":"nuclear RNA export factor 5","omim_gene":["300319"],"alias_name":null,"gene_symbol":"NXF5","hgnc_symbol":"NXF5","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"X:101087085-101112549","ensembl_id":"ENSG00000126952"}},"GRch38":{"90":{"location":"X:101832112-101857577","ensembl_id":"ENSG00000126952"}}},"hgnc_date_symbol_changed":"2000-07-31"},"entity_type":"gene","entity_name":"NXF5","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["11566096","26350204","23675524","22030050"],"evidence":["Expert Review Red"],"phenotypes":["Intellectual Disability"],"mode_of_inheritance":"X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","tags":[],"panel":{"id":285,"hash_id":"558aa423bb5a16630e15b63c","name":"Intellectual disability","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neurodevelopmental disorders","status":"public","version":"2.1065","version_created":"2019-10-07T13:42:16.019766Z","relevant_disorders":["Coarse facial features including Coffin-Siris-like disorders","ID","Moderate","severe or profound intellectual disability","Schizophrenia plus additional features","Intellectual disability - microarray","fragile X and sequencing"],"stats":{"number_of_genes":2253,"number_of_strs":11,"number_of_regions":57},"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."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:8075","gene_name":"nuclear RNA export factor 5","omim_gene":["300319"],"alias_name":null,"gene_symbol":"NXF5","hgnc_symbol":"NXF5","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"X:101087085-101112549","ensembl_id":"ENSG00000126952"}},"GRch38":{"90":{"location":"X:101832112-101857577","ensembl_id":"ENSG00000126952"}}},"hgnc_date_symbol_changed":"2000-07-31"},"entity_type":"gene","entity_name":"NXF5","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["23686279"],"evidence":["NHS GMS"],"phenotypes":["FSGS","heart-block disorder"],"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)"}]}}]}