{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA0155","TSBP","p150TSP"],"biotype":"protein_coding","hgnc_id":"HGNC:16850","gene_name":"CTR9 homolog, Paf1/RNA polymerase II complex component","omim_gene":["609366"],"alias_name":null,"gene_symbol":"CTR9","hgnc_symbol":"CTR9","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"11:10772534-10801290","ensembl_id":"ENSG00000198730"}},"GRch38":{"90":{"location":"11:10750987-10779743","ensembl_id":"ENSG00000198730"}}},"hgnc_date_symbol_changed":"2006-05-22"},"entity_type":"gene","entity_name":"CTR9","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["25099282","29292210"],"evidence":["Expert list","Expert Review Green"],"phenotypes":["Familial Wilms tumor"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":243,"hash_id":"55af539322c1fc78a9ef5052","name":"Tumour predisposition - childhood onset","disease_group":"Tumour syndromes","disease_sub_group":"Childhood Tumours","status":"public","version":"1.36","version_created":"2019-08-12T08:35:21.843722Z","relevant_disorders":["Paediatric congenital malformation-dysmorphism-tumour syndrome","Paediatric congenital malformation-dysmorphism-tumour syndromes","Paediatric congenital malformation-dysmorphism-tumour sydromes","Paediatric congenital malformation-dysmorphism-tumour syndrome","R359"],"stats":{"number_of_genes":113,"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 Cancer Germline Virtual","slug":"gms-cancer-germline-virtual","description":"This is a panel used for WGS germline analysis for the GMS."}]}}]}