{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["INK4C","p18"],"biotype":"protein_coding","hgnc_id":"HGNC:1789","gene_name":"cyclin dependent kinase inhibitor 2C","omim_gene":["603369"],"alias_name":null,"gene_symbol":"CDKN2C","hgnc_symbol":"CDKN2C","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:51426417-51440305","ensembl_id":"ENSG00000123080"}},"GRch38":{"90":{"location":"1:50960745-50974633","ensembl_id":"ENSG00000123080"}}},"hgnc_date_symbol_changed":"1995-07-06"},"entity_type":"gene","entity_name":"CDKN2C","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["19141585"],"evidence":["Expert Review Red","UKGTN"],"phenotypes":["No OMIM number","Multiple endocrine neoplasia 1"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":480,"hash_id":null,"name":"Familial hyperparathyroidism","disease_group":"","disease_sub_group":"","status":"public","version":"2.1","version_created":"2019-09-10T17:12:48.944602Z","relevant_disorders":["R151"],"stats":{"number_of_genes":10,"number_of_strs":0,"number_of_regions":0},"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."}]}}]}