{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA0558"],"biotype":"protein_coding","hgnc_id":"HGNC:1400","gene_name":"calcium voltage-gated channel auxiliary subunit alpha2delta 2","omim_gene":["607082"],"alias_name":["gene 26"],"gene_symbol":"CACNA2D2","hgnc_symbol":"CACNA2D2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:50400233-50541675","ensembl_id":"ENSG00000007402"}},"GRch38":{"90":{"location":"3:50362799-50504244","ensembl_id":"ENSG00000007402"}}},"hgnc_date_symbol_changed":"1999-06-11"},"entity_type":"gene","entity_name":"CACNA2D2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["24358150","23339110","11487633","11756448"],"evidence":["Wessex and West Midlands GLH","NHS GMS","Expert Review Amber","Victorian Clinical Genetics Services"],"phenotypes":["Absence epilepsy"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":["watchlist"],"panel":{"id":402,"hash_id":null,"name":"Genetic epilepsy syndromes","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Inherited Epilepsy Syndromes","status":"public","version":"1.363","version_created":"2019-10-08T10:06:11.607307Z","relevant_disorders":["Epilepsy Plus","Epilepsy plus other features","Genetic Epilepsy Syndromes","Epileptic encephalopathy","Familial Focal Epilepsies","Familial Genetic Generalised Epilepsies","Genetic Epilepsies with Febrile Seizures Plus (GEFS+)","Genetic Epilepsies with Febrile Seizures Plus"],"stats":{"number_of_genes":614,"number_of_strs":2,"number_of_regions":13},"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)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":["KIAA0558"],"biotype":"protein_coding","hgnc_id":"HGNC:1400","gene_name":"calcium voltage-gated channel auxiliary subunit alpha2delta 2","omim_gene":["607082"],"alias_name":["gene 26"],"gene_symbol":"CACNA2D2","hgnc_symbol":"CACNA2D2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:50400233-50541675","ensembl_id":"ENSG00000007402"}},"GRch38":{"90":{"location":"3:50362799-50504244","ensembl_id":"ENSG00000007402"}}},"hgnc_date_symbol_changed":"1999-06-11"},"entity_type":"gene","entity_name":"CACNA2D2","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":null,"publications":["23339110","24358150","30410802","29997391","31402629","11487633","11756448","4177347","14660671","15331424"],"evidence":["Expert Review Amber","Literature"],"phenotypes":["Cerebellar atrophy with seizures and variable developmental delay, 618501"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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"}]}}]}