{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["STK1","FLK2","CD135"],"biotype":"protein_coding","hgnc_id":"HGNC:3765","gene_name":"fms related tyrosine kinase 3","omim_gene":["136351"],"alias_name":null,"gene_symbol":"FLT3","hgnc_symbol":"FLT3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"13:28577411-28674729","ensembl_id":"ENSG00000122025"}},"GRch38":{"90":{"location":"13:28003274-28100592","ensembl_id":"ENSG00000122025"}}},"hgnc_date_symbol_changed":"1990-07-30"},"entity_type":"gene","entity_name":"FLT3","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["15390271"],"evidence":["Expert Review Amber","BRIDGE consortium (NIHRBR-RD)"],"phenotypes":["Myelodysplastic syndrome (MDS), Paediatric"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","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"}]}}]}