{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["ATF6A"],"biotype":"protein_coding","hgnc_id":"HGNC:791","gene_name":"activating transcription factor 6","omim_gene":["605537"],"alias_name":["activating transcription factor 6 alpha"],"gene_symbol":"ATF6","hgnc_symbol":"ATF6","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:161736084-161933860","ensembl_id":"ENSG00000118217"}},"GRch38":{"90":{"location":"1:161766294-161964070","ensembl_id":"ENSG00000118217"}}},"hgnc_date_symbol_changed":"1999-12-15"},"entity_type":"gene","entity_name":"ATF6","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26063662","26029869"],"evidence":["ClinGen","Expert Review Green","Other"],"phenotypes":["Achromatopsia"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":64,"hash_id":"58ee38f88f62033bda307d54","name":"ClinGen Gene Validity Curations","disease_group":"","disease_sub_group":"","status":"public","version":"0.64","version_created":"2019-06-20T15:10:34.572009Z","relevant_disorders":[],"stats":{"number_of_genes":47,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"ClinGen Curated genes","slug":"clingen-curated-genes","description":"ClinGen Curated genes"}]}},{"gene_data":{"alias":["ATF6A"],"biotype":"protein_coding","hgnc_id":"HGNC:791","gene_name":"activating transcription factor 6","omim_gene":["605537"],"alias_name":["activating transcription factor 6 alpha"],"gene_symbol":"ATF6","hgnc_symbol":"ATF6","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:161736084-161933860","ensembl_id":"ENSG00000118217"}},"GRch38":{"90":{"location":"1:161766294-161964070","ensembl_id":"ENSG00000118217"}}},"hgnc_date_symbol_changed":"1999-12-15"},"entity_type":"gene","entity_name":"ATF6","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26063662","26029869"],"evidence":["NHS GMS","Expert Review Green"],"phenotypes":["Achromatopsia 7"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":307,"hash_id":"56e0238b22c1fc09c97a6e46","name":"Retinal disorders","disease_group":"Ophthalmological disorders","disease_sub_group":"Posterior segment abnormalities","status":"public","version":"1.199","version_created":"2019-10-08T09:22:18.436205Z","relevant_disorders":["Posterior segment abnormalities","Cone Dysfunction Syndrome","Developmental macular and foveal dystrophy","Inherited macular dystrophy","Leber Congenital Amaurosis Early-Onset Severe Retinal Dystrophy","Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy","Leber Congenital Amaurosis or Early-Onset Severe Retinal Dystrophy","Rod Dysfunction Syndrome","Rod-cone dystrophy","Familial exudative vitreoretinopathy","Familial exudative retinopathy","R32","R33","R34","R35"],"stats":{"number_of_genes":320,"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."}]}}]}