{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["B23","NPM"],"biotype":"protein_coding","hgnc_id":"HGNC:7910","gene_name":"nucleophosmin 1","omim_gene":["164040"],"alias_name":["nucleolar phosphoprotein B23","numatrin","nucleophosmin/nucleoplasmin family, member 1"],"gene_symbol":"NPM1","hgnc_symbol":"NPM1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"5:170814120-170838141","ensembl_id":"ENSG00000181163"}},"GRch38":{"90":{"location":"5:171387116-171411137","ensembl_id":"ENSG00000181163"}}},"hgnc_date_symbol_changed":"1993-08-24"},"entity_type":"gene","entity_name":"NPM1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","BRIDGE consortium (NIHRBR-RD)"],"phenotypes":["Acute myeloid leukaemia (AML)"],"mode_of_inheritance":"Unknown","tags":["somatic"],"panel":{"id":159,"hash_id":"58a70e858f62037e8779b2e8","name":"Cytopenias and congenital anaemias","disease_group":"Haematological disorders","disease_sub_group":"Anaemias and red cell disorders","status":"public","version":"1.73","version_created":"2019-09-23T11:25:32.403071Z","relevant_disorders":["Aplastic anaemia with or without paroxysmal nocturnal haemoglobinuria","Apparent aplastic anaemia or paroxysmal nocturnal haemoglobinuria","Congenital anaemias","Early onset pancytopenia and red cell disorders","Anaemias and red cell disorders","Cytopaenias and congenital anaemias","Cytopenia and pancytopenia"],"stats":{"number_of_genes":219,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}