{"count":6,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA0458","ARP","ARG","DNB1"],"biotype":"protein_coding","hgnc_id":"HGNC:9965","gene_name":"arginine-glutamic acid dipeptide repeats","omim_gene":["605226"],"alias_name":null,"gene_symbol":"RERE","hgnc_symbol":"RERE","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:8412457-8877702","ensembl_id":"ENSG00000142599"}},"GRch38":{"90":{"location":"1:8352397-8817643","ensembl_id":"ENSG00000142599"}}},"hgnc_date_symbol_changed":"2000-05-19"},"entity_type":"gene","entity_name":"RERE","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."}]}},{"gene_data":{"alias":["KIAA0458","ARP","ARG","DNB1"],"biotype":"protein_coding","hgnc_id":"HGNC:9965","gene_name":"arginine-glutamic acid dipeptide repeats","omim_gene":["605226"],"alias_name":null,"gene_symbol":"RERE","hgnc_symbol":"RERE","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:8412457-8877702","ensembl_id":"ENSG00000142599"}},"GRch38":{"90":{"location":"1:8352397-8817643","ensembl_id":"ENSG00000142599"}}},"hgnc_date_symbol_changed":"2000-05-19"},"entity_type":"gene","entity_name":"RERE","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["PAGE DD-Gene2Phenotype","Expert Review Green"],"phenotypes":["Phenocopy of Proximal 1p36 Deletions"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":478,"hash_id":null,"name":"Fetal anomalies","disease_group":"","disease_sub_group":"","status":"public","version":"0.344","version_created":"2019-09-17T09:38:10.568007Z","relevant_disorders":["R21"],"stats":{"number_of_genes":1721,"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."}]}},{"gene_data":{"alias":["KIAA0458","ARP","ARG","DNB1"],"biotype":"protein_coding","hgnc_id":"HGNC:9965","gene_name":"arginine-glutamic acid dipeptide repeats","omim_gene":["605226"],"alias_name":null,"gene_symbol":"RERE","hgnc_symbol":"RERE","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:8412457-8877702","ensembl_id":"ENSG00000142599"}},"GRch38":{"90":{"location":"1:8352397-8817643","ensembl_id":"ENSG00000142599"}}},"hgnc_date_symbol_changed":"2000-05-19"},"entity_type":"gene","entity_name":"RERE","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["27087320"],"evidence":["DD-Gene2Phenotype","Expert Review Green"],"phenotypes":["Phenocopy of Proximal 1p36 Deletions"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"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":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":["KIAA0458","ARP","ARG","DNB1"],"biotype":"protein_coding","hgnc_id":"HGNC:9965","gene_name":"arginine-glutamic acid dipeptide repeats","omim_gene":["605226"],"alias_name":null,"gene_symbol":"RERE","hgnc_symbol":"RERE","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:8412457-8877702","ensembl_id":"ENSG00000142599"}},"GRch38":{"90":{"location":"1:8352397-8817643","ensembl_id":"ENSG00000142599"}}},"hgnc_date_symbol_changed":"2000-05-19"},"entity_type":"gene","entity_name":"RERE","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27087320","25529582"],"evidence":["Expert Review Green","Victorian Clinical Genetics Services","BRIDGE study SPEED NEURO Tier1 Gene"],"phenotypes":["Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart 616975"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":285,"hash_id":"558aa423bb5a16630e15b63c","name":"Intellectual disability","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neurodevelopmental disorders","status":"public","version":"2.1065","version_created":"2019-10-07T13:42:16.019766Z","relevant_disorders":["Coarse facial features including Coffin-Siris-like disorders","ID","Moderate","severe or profound intellectual disability","Schizophrenia plus additional features","Intellectual disability - microarray","fragile X and sequencing"],"stats":{"number_of_genes":2253,"number_of_strs":11,"number_of_regions":57},"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":["KIAA0458","ARP","ARG","DNB1"],"biotype":"protein_coding","hgnc_id":"HGNC:9965","gene_name":"arginine-glutamic acid dipeptide repeats","omim_gene":["605226"],"alias_name":null,"gene_symbol":"RERE","hgnc_symbol":"RERE","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:8412457-8877702","ensembl_id":"ENSG00000142599"}},"GRch38":{"90":{"location":"1:8352397-8817643","ensembl_id":"ENSG00000142599"}}},"hgnc_date_symbol_changed":"2000-05-19"},"entity_type":"gene","entity_name":"RERE","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["27087320","29330883"],"evidence":["NHS GMS","Expert Review Green","London North GLH"],"phenotypes":["Neurodevelopment Disorder with anomalies of the Brain, Eye and/or Heart, NEDBEH, 616975"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":509,"hash_id":null,"name":"Structural eye disease","disease_group":"","disease_sub_group":"","status":"public","version":"0.93","version_created":"2019-10-09T13:18:12.923145Z","relevant_disorders":["R36"],"stats":{"number_of_genes":456,"number_of_strs":0,"number_of_regions":2},"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)"}]}},{"gene_data":{"alias":["KIAA0458","ARP","ARG","DNB1"],"biotype":"protein_coding","hgnc_id":"HGNC:9965","gene_name":"arginine-glutamic acid dipeptide repeats","omim_gene":["605226"],"alias_name":null,"gene_symbol":"RERE","hgnc_symbol":"RERE","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:8412457-8877702","ensembl_id":"ENSG00000142599"}},"GRch38":{"90":{"location":"1:8352397-8817643","ensembl_id":"ENSG00000142599"}}},"hgnc_date_symbol_changed":"2000-05-19"},"entity_type":"gene","entity_name":"RERE","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Expert review red","Literature"],"phenotypes":["Congenital or cystic renal disease","MIM 616975","Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":720,"hash_id":null,"name":"Groopman et al 2019 - Genes with diagnostic variants","disease_group":"","disease_sub_group":"","status":"public","version":"0.8","version_created":"2019-07-09T15:48:14.145108Z","relevant_disorders":[],"stats":{"number_of_genes":66,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Submitted List","slug":"submitted-list","description":"Original list, ratings, comments submitted to PanelApp- generally used for the creation of reference GMS panels, these panels  should be internal only"}]}}]}