{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["DFNB61"],"biotype":"protein_coding","hgnc_id":"HGNC:9359","gene_name":"solute carrier family 26 member 5","omim_gene":["604943"],"alias_name":["deafness, neurosensory, autosomal recessive, 61"],"gene_symbol":"SLC26A5","hgnc_symbol":"SLC26A5","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"7:102993177-103086624","ensembl_id":"ENSG00000170615"}},"GRch38":{"90":{"location":"7:103352730-103446177","ensembl_id":"ENSG00000170615"}}},"hgnc_date_symbol_changed":"2005-09-13"},"entity_type":"gene","entity_name":"SLC26A5","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["25262649","10821263","11423665","11867734","12239568","12719379","16086836","17998209","18776049","19492055","21689600","23212912","24164807","25262649","24164807","6824437","26969326"],"evidence":["Expert Review Green","Expert","Radboud University Medical Center, Nijmegen","Emory Genetics Laboratory","UKGTN","Illumina TruGenome Clinical Sequencing Services"],"phenotypes":["#613865:?Deafness, autosomal recessive 61","Nonsyndromic Hearing Loss, Recessive","Deafness, autosomal recessive 61, 613865","hearing loss"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":126,"hash_id":"558ac48fbb5a16630dcfeaad","name":"Hearing loss","disease_group":"Hearing and ear disorders","disease_sub_group":"Non-syndromic hearing loss","status":"public","version":"2.2","version_created":"2019-09-03T14:01:56.987667Z","relevant_disorders":["Congenital hearing impairment","Autosomal dominant deafness","Congenital hearing impairment (profound/severe)","R67"],"stats":{"number_of_genes":358,"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."},{"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)"}]}}]}