{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MGC10561"],"biotype":"protein_coding","hgnc_id":"HGNC:1552","gene_name":"chromobox 2","omim_gene":["602770"],"alias_name":["Pc class homolog (Drosophila)"],"gene_symbol":"CBX2","hgnc_symbol":"CBX2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"17:77751931-77761782","ensembl_id":"ENSG00000173894"}},"GRch38":{"90":{"location":"17:79778132-79787983","ensembl_id":"ENSG00000173894"}}},"hgnc_date_symbol_changed":"1994-05-25"},"entity_type":"gene","entity_name":"CBX2","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["23219007","19361780"],"evidence":["Expert Review Red","UKGTN","Radboud University Medical Center, Nijmegen","Other"],"phenotypes":["Gender Assignment Gene Panel (UKGTN)","46XY sex reversal 5, 613080"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":9,"hash_id":"569380ac22c1fc251660faf8","name":"Disorders of sex development","disease_group":"Endocrine disorders","disease_sub_group":"Gonadal and sex development disorders","status":"public","version":"2.1","version_created":"2019-10-01T10:16:03.440399Z","relevant_disorders":["R146"],"stats":{"number_of_genes":54,"number_of_strs":0,"number_of_regions":1},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}