{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["NPR2L","NPR2"],"biotype":"protein_coding","hgnc_id":"HGNC:24969","gene_name":"NPR2 like, GATOR1 complex subunit","omim_gene":["607072"],"alias_name":null,"gene_symbol":"NPRL2","hgnc_symbol":"NPRL2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:50384761-50388522","ensembl_id":"ENSG00000114388"}},"GRch38":{"90":{"location":"3:50347330-50351091","ensembl_id":"ENSG00000114388"}}},"hgnc_date_symbol_changed":"2010-03-30"},"entity_type":"gene","entity_name":"NPRL2","confidence_level":"2","penetrance":"Incomplete","mode_of_pathogenicity":null,"publications":["26505888","27173016","30093711"],"evidence":["Wessex and West Midlands GLH","NHS GMS","Expert Review Amber","Expert Review"],"phenotypes":["Epilepsy, familial focal, with variable foci 2, 617116"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","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"}]}}]}