{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CPR4"],"biotype":"protein_coding","hgnc_id":"HGNC:1596","gene_name":"cyclin K","omim_gene":["603544"],"alias_name":null,"gene_symbol":"CCNK","hgnc_symbol":"CCNK","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"14:99947506-100001381","ensembl_id":"ENSG00000090061"}},"GRch38":{"90":{"location":"14:99481169-99535044","ensembl_id":"ENSG00000090061"}}},"hgnc_date_symbol_changed":"1998-12-22"},"entity_type":"gene","entity_name":"CCNK","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["30122539"],"evidence":["Expert Review Red","DD-Gene2Phenotype"],"phenotypes":["Syndromic Neurodevelopmental Disorder with Distinctive Facial Dysmorphism"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}