{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ20032"],"biotype":"protein_coding","hgnc_id":"HGNC:25941","gene_name":"tet methylcytosine dioxygenase 2","omim_gene":["612839"],"alias_name":null,"gene_symbol":"TET2","hgnc_symbol":"TET2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:106067032-106200973","ensembl_id":"ENSG00000168769"}},"GRch38":{"90":{"location":"4:105145875-105279816","ensembl_id":"ENSG00000168769"}}},"hgnc_date_symbol_changed":"2008-03-12"},"entity_type":"gene","entity_name":"TET2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","SFARI"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":657,"hash_id":null,"name":"Autism","disease_group":"","disease_sub_group":"","status":"public","version":"0.15","version_created":"2019-06-20T15:10:14.437740Z","relevant_disorders":[],"stats":{"number_of_genes":733,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Research","slug":"research","description":"This is a gene panel used for research."}]}},{"gene_data":{"alias":["FLJ20032"],"biotype":"protein_coding","hgnc_id":"HGNC:25941","gene_name":"tet methylcytosine dioxygenase 2","omim_gene":["612839"],"alias_name":null,"gene_symbol":"TET2","hgnc_symbol":"TET2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"4:106067032-106200973","ensembl_id":"ENSG00000168769"}},"GRch38":{"90":{"location":"4:105145875-105279816","ensembl_id":"ENSG00000168769"}}},"hgnc_date_symbol_changed":"2008-03-12"},"entity_type":"gene","entity_name":"TET2","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["Myelodysplastic syndrome, somatic, 614286"],"mode_of_inheritance":"Other - please specify in evaluation comments","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"}]}}]}