{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["SC-35","SC35","PR264","SFRS2A"],"biotype":"protein_coding","hgnc_id":"HGNC:10783","gene_name":"serine and arginine rich splicing factor 2","omim_gene":["600813"],"alias_name":["SR splicing factor 2"],"gene_symbol":"SRSF2","hgnc_symbol":"SRSF2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"17:74730197-74733456","ensembl_id":"ENSG00000161547"}},"GRch38":{"90":{"location":"17:76734115-76737374","ensembl_id":"ENSG00000161547"}}},"hgnc_date_symbol_changed":"2010-06-22"},"entity_type":"gene","entity_name":"SRSF2","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["22238327","22343734","22389253"],"evidence":["Expert Review Red","BRIDGE consortium (NIHRBR-RD)"],"phenotypes":["Myelodysplastic syndrome (MDS), Paediatric"],"mode_of_inheritance":"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"}]}}]}