{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["VDUP1","EST01027","HHCPA78","THIF","ARRDC6"],"biotype":null,"hgnc_id":"HGNC:16952","gene_name":"thioredoxin interacting protein","omim_gene":["606599"],"alias_name":["upregulated by 1,25-dihydroxyvitamin D-3","thioredoxin binding protein 2"],"gene_symbol":"TXNIP","hgnc_symbol":"TXNIP","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:145438469-145442635","ensembl_id":"ENSG00000117289"}},"GRch38":{"90":{"location":"1:145992435-145996600","ensembl_id":"ENSG00000265972"}}},"hgnc_date_symbol_changed":"2001-12-12"},"entity_type":"gene","entity_name":"TXNIP","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","UKGTN"],"phenotypes":["Thrombocytopenia Absent-Radius Syndrome"],"mode_of_inheritance":"","tags":[],"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"}]}}]}