{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA0307","bHLHe1"],"biotype":"protein_coding","hgnc_id":"HGNC:16876","gene_name":"aryl hydrocarbon receptor nuclear translocator 2","omim_gene":["606036"],"alias_name":null,"gene_symbol":"ARNT2","hgnc_symbol":"ARNT2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"15:80696692-80890278","ensembl_id":"ENSG00000172379"}},"GRch38":{"90":{"location":"15:80404350-80597937","ensembl_id":"ENSG00000172379"}}},"hgnc_date_symbol_changed":"2001-12-05"},"entity_type":"gene","entity_name":"ARNT2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["24022475"],"evidence":["Expert Review Red","Radboud University Medical Center"],"phenotypes":["?Webb-Dattani syndrome (615926)"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":483,"hash_id":null,"name":"Pituitary hormone deficiency","disease_group":"","disease_sub_group":"","status":"public","version":"2.0","version_created":"2019-07-31T14:30:21.964840Z","relevant_disorders":["R159"],"stats":{"number_of_genes":50,"number_of_strs":0,"number_of_regions":0},"types":[{"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."}]}},{"gene_data":{"alias":["KIAA0307","bHLHe1"],"biotype":"protein_coding","hgnc_id":"HGNC:16876","gene_name":"aryl hydrocarbon receptor nuclear translocator 2","omim_gene":["606036"],"alias_name":null,"gene_symbol":"ARNT2","hgnc_symbol":"ARNT2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"15:80696692-80890278","ensembl_id":"ENSG00000172379"}},"GRch38":{"90":{"location":"15:80404350-80597937","ensembl_id":"ENSG00000172379"}}},"hgnc_date_symbol_changed":"2001-12-05"},"entity_type":"gene","entity_name":"ARNT2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","SFARI"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":657,"hash_id":null,"name":"Autism","disease_group":"","disease_sub_group":"","status":"public","version":"0.15","version_created":"2019-06-20T15:10:14.437740Z","relevant_disorders":[],"stats":{"number_of_genes":733,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Research","slug":"research","description":"This is a gene panel used for research."}]}}]}