{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PLSTIRE"],"biotype":"protein_coding","hgnc_id":"HGNC:1777","gene_name":"cyclin dependent kinase 6","omim_gene":["603368"],"alias_name":null,"gene_symbol":"CDK6","hgnc_symbol":"CDK6","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"7:92234235-92465908","ensembl_id":"ENSG00000105810"}},"GRch38":{"90":{"location":"7:92604921-92836594","ensembl_id":"ENSG00000105810"}}},"hgnc_date_symbol_changed":"1994-02-14"},"entity_type":"gene","entity_name":"CDK6","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["25951892","25548773","23918663"],"evidence":["NHS GMS","Other","Literature"],"phenotypes":["Autosomal recessive primary microcephaly (MCPH)","?Microcephaly 12, primary, autosomal recessive, 616080"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":162,"hash_id":"568f860222c1fc1c79ca1769","name":"Severe microcephaly","disease_group":"Dysmorphic and congenital abnormality syndromes","disease_sub_group":"DNA repair disorders","status":"public","version":"1.72","version_created":"2019-08-19T16:58:29.143286Z","relevant_disorders":["Primary Microcephaly - Microcephalic Dwarfism Spectrum","Severe microcephaly"],"stats":{"number_of_genes":122,"number_of_strs":0,"number_of_regions":5},"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."}]}}]}