{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["EMTB","S14"],"biotype":"protein_coding","hgnc_id":"HGNC:10387","gene_name":"ribosomal protein S14","omim_gene":["130620"],"alias_name":["emetine resistance","40S ribosomal protein S14"],"gene_symbol":"RPS14","hgnc_symbol":"RPS14","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"5:149822753-149829319","ensembl_id":"ENSG00000164587"}},"GRch38":{"90":{"location":"5:150443190-150449756","ensembl_id":"ENSG00000164587"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"RPS14","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["Macrocyticanemia,refractory,dueto5qdeletion,somatic,153550  3","Macrocytic anemia, refractory, due to 5q deletion, somatic, 153550 -3"],"mode_of_inheritance":"","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"}]}}]}