{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ12042","MESRGP","BOR","DasraB"],"biotype":"protein_coding","hgnc_id":"HGNC:14629","gene_name":"cell division cycle associated 8","omim_gene":["609977"],"alias_name":["borealin"],"gene_symbol":"CDCA8","hgnc_symbol":"CDCA8","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:38158090-38175391","ensembl_id":"ENSG00000134690"}},"GRch38":{"90":{"location":"1:37692418-37709719","ensembl_id":"ENSG00000134690"}}},"hgnc_date_symbol_changed":"2002-04-03"},"entity_type":"gene","entity_name":"CDCA8","confidence_level":"2","penetrance":"unknown","mode_of_pathogenicity":"Other","publications":["28025328","29546359"],"evidence":["Expert Review Amber","NHS GMS","Expert Review","Literature"],"phenotypes":["Congenital hypothyroidism","thyroid dysgenesis","No OMIM number"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","tags":[],"panel":{"id":31,"hash_id":"5763f2938f620350a1996046","name":"Congenital hypothyroidism","disease_group":"Endocrine disorders","disease_sub_group":"Thyroid disorders","status":"public","version":"2.0","version_created":"2019-07-31T13:52:41.584963Z","relevant_disorders":["Congenital hypothyroidism or thyroid agenesis","R145"],"stats":{"number_of_genes":34,"number_of_strs":0,"number_of_regions":2},"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."}]}}]}