{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["VR22","MGC26194"],"biotype":"protein_coding","hgnc_id":"HGNC:2511","gene_name":"catenin alpha 3","omim_gene":["607667"],"alias_name":["alpha-T-catenin"],"gene_symbol":"CTNNA3","hgnc_symbol":"CTNNA3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"10:67672276-69455927","ensembl_id":"ENSG00000183230"}},"GRch38":{"90":{"location":"10:65912518-67696169","ensembl_id":"ENSG00000183230"}}},"hgnc_date_symbol_changed":"2000-03-29"},"entity_type":"gene","entity_name":"CTNNA3","confidence_level":"0","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Removed","Other","Emory Genetics Laboratory"],"phenotypes":["Arrhythmias","Arrhythmogenic right ventricular dysplasia, familial, 13,  615616"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":45,"hash_id":"5763f6508f620350a1996055","name":"Sudden death in young people","disease_group":"Cardiovascular disorders","disease_sub_group":"Cardiac arrhythmia","status":"public","version":"1.12","version_created":"2019-06-20T15:15:17.414434Z","relevant_disorders":["Unexplained sudden death in the young"],"stats":{"number_of_genes":35,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["VR22","MGC26194"],"biotype":"protein_coding","hgnc_id":"HGNC:2511","gene_name":"catenin alpha 3","omim_gene":["607667"],"alias_name":["alpha-T-catenin"],"gene_symbol":"CTNNA3","hgnc_symbol":"CTNNA3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"10:67672276-69455927","ensembl_id":"ENSG00000183230"}},"GRch38":{"90":{"location":"10:65912518-67696169","ensembl_id":"ENSG00000183230"}}},"hgnc_date_symbol_changed":"2000-03-29"},"entity_type":"gene","entity_name":"CTNNA3","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["South West GLH","Expert Review Red","Radboud University Medical Center, Nijmegen","Expert list"],"phenotypes":["Arrhythmogenic right ventricular dysplasia, familial, 13,"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":134,"hash_id":"55a3876e22c1fc63fec6d0da","name":"Arrhythmogenic cardiomyopathy","disease_group":"Cardiovascular disorders","disease_sub_group":"Cardiomyopathy","status":"public","version":"1.41","version_created":"2019-10-03T13:27:28.690231Z","relevant_disorders":["Arrhythmogenic Right Ventricular Cardiomyopathy","Arrythmogenic cardiomyopathy","R133"],"stats":{"number_of_genes":19,"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","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)"}]}},{"gene_data":{"alias":["VR22","MGC26194"],"biotype":"protein_coding","hgnc_id":"HGNC:2511","gene_name":"catenin alpha 3","omim_gene":["607667"],"alias_name":["alpha-T-catenin"],"gene_symbol":"CTNNA3","hgnc_symbol":"CTNNA3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"10:67672276-69455927","ensembl_id":"ENSG00000183230"}},"GRch38":{"90":{"location":"10:65912518-67696169","ensembl_id":"ENSG00000183230"}}},"hgnc_date_symbol_changed":"2000-03-29"},"entity_type":"gene","entity_name":"CTNNA3","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."}]}}]}
