{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["hTg737","Tg737","D13S1056E","MGC26259"],"biotype":"protein_coding","hgnc_id":"HGNC:20606","gene_name":"intraflagellar transport 88","omim_gene":["600595"],"alias_name":["polaris homolog"],"gene_symbol":"IFT88","hgnc_symbol":"IFT88","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"13:21140585-21265503","ensembl_id":"ENSG00000032742"}},"GRch38":{"90":{"location":"13:20567069-20691437","ensembl_id":"ENSG00000032742"}}},"hgnc_date_symbol_changed":"2005-11-02"},"entity_type":"gene","entity_name":"IFT88","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["23034798"],"evidence":["Expert Review Red","UKGTN","Expert list"],"phenotypes":[],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":309,"hash_id":"5693952f22c1fc251660fb1e","name":"Skeletal dysplasia","disease_group":"Skeletal disorders","disease_sub_group":"Skeletal dysplasias","status":"public","version":"1.203","version_created":"2019-10-03T09:38:50.417968Z","relevant_disorders":["Unexplained skeletal dysplasia","Skeletal dysplasia"],"stats":{"number_of_genes":546,"number_of_strs":1,"number_of_regions":6},"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":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":["hTg737","Tg737","D13S1056E","MGC26259"],"biotype":"protein_coding","hgnc_id":"HGNC:20606","gene_name":"intraflagellar transport 88","omim_gene":["600595"],"alias_name":["polaris homolog"],"gene_symbol":"IFT88","hgnc_symbol":"IFT88","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"13:21140585-21265503","ensembl_id":"ENSG00000032742"}},"GRch38":{"90":{"location":"13:20567069-20691437","ensembl_id":"ENSG00000032742"}}},"hgnc_date_symbol_changed":"2005-11-02"},"entity_type":"gene","entity_name":"IFT88","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert"],"phenotypes":[],"mode_of_inheritance":"","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)"}]}}]}