{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CAG4A"],"biotype":"protein_coding","hgnc_id":"HGNC:11968","gene_name":"canopy FGF signaling regulator 3","omim_gene":["610774"],"alias_name":null,"gene_symbol":"CNPY3","hgnc_symbol":"CNPY3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:42896938-42907025","ensembl_id":"ENSG00000137161"}},"GRch38":{"90":{"location":"6:42929192-42939287","ensembl_id":"ENSG00000137161"}}},"hgnc_date_symbol_changed":"2007-10-22"},"entity_type":"gene","entity_name":"CNPY3","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["29394991"],"evidence":["Expert Review Amber","DD-Gene2Phenotype"],"phenotypes":["EARLY ONSET EPILEPTIC ENCEPHALOPATHY"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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":["CAG4A"],"biotype":"protein_coding","hgnc_id":"HGNC:11968","gene_name":"canopy FGF signaling regulator 3","omim_gene":["610774"],"alias_name":null,"gene_symbol":"CNPY3","hgnc_symbol":"CNPY3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:42896938-42907025","ensembl_id":"ENSG00000137161"}},"GRch38":{"90":{"location":"6:42929192-42939287","ensembl_id":"ENSG00000137161"}}},"hgnc_date_symbol_changed":"2007-10-22"},"entity_type":"gene","entity_name":"CNPY3","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["29394991"],"evidence":["Expert Review Green","Wessex and West Midlands GLH","NHS GMS","Victorian Clinical Genetics Services"],"phenotypes":["Epileptic encephalopathy, early infantile, 60 617929"],"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"}]}}]}