{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["bHLHe76"],"biotype":"protein_coding","hgnc_id":"HGNC:348","gene_name":"aryl hydrocarbon receptor","omim_gene":["600253"],"alias_name":null,"gene_symbol":"AHR","hgnc_symbol":"AHR","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:17338246-17385776","ensembl_id":"ENSG00000106546"}},"GRch38":{"90":{"location":"7:17298622-17346152","ensembl_id":"ENSG00000106546"}}},"hgnc_date_symbol_changed":"1993-05-18"},"entity_type":"gene","entity_name":"AHR","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["28851966","31009037","23301081"],"evidence":["Expert Review Amber","Expert list"],"phenotypes":["?Retinitis pigmentosa 85, 618345","Foveal hypoplasia without albinism","Infantile nystagmus"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":511,"hash_id":null,"name":"Albinism or congenital nystagmus","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-08-05T09:16:46.441760Z","relevant_disorders":["R39"],"stats":{"number_of_genes":41,"number_of_strs":0,"number_of_regions":0},"types":[{"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)"},{"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."}]}}]}