{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MAR"],"biotype":"protein_coding","hgnc_id":"HGNC:6116","gene_name":"interferon regulatory factor 1","omim_gene":["147575"],"alias_name":["interferon regulatory factor-1"],"gene_symbol":"IRF1","hgnc_symbol":"IRF1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"5:131817301-131826490","ensembl_id":"ENSG00000125347"}},"GRch38":{"90":{"location":"5:132481609-132490798","ensembl_id":"ENSG00000125347"}}},"hgnc_date_symbol_changed":"1991-05-09"},"entity_type":"gene","entity_name":"IRF1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["Myelodysplastic syndrome, preleukemic","Myelogenous leukemia, acute","Gastric cancer, somatic, 613659","Nonsmall cell lung cancer, somatic, 211980"],"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"}]}}]}