{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["SCARB3","GPIV","FAT","GP4","GP3B"],"biotype":"protein_coding","hgnc_id":"HGNC:1663","gene_name":"CD36 molecule","omim_gene":["173510"],"alias_name":null,"gene_symbol":"CD36","hgnc_symbol":"CD36","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"7:79998891-80308593","ensembl_id":"ENSG00000135218"}},"GRch38":{"90":{"location":"7:80369575-80679277","ensembl_id":"ENSG00000135218"}}},"hgnc_date_symbol_changed":"1993-06-04"},"entity_type":"gene","entity_name":"CD36","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["[Macrothrombocytopenia] (1)"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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"}]}}]}