{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["ANOVA"],"biotype":"protein_coding","hgnc_id":"HGNC:7887","gene_name":"NOVA alternative splicing regulator 2","omim_gene":["601991"],"alias_name":["neuro-oncological ventral antigen 3"],"gene_symbol":"NOVA2","hgnc_symbol":"NOVA2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:46436992-46476804","ensembl_id":"ENSG00000104967"}},"GRch38":{"90":{"location":"19:45933734-45973546","ensembl_id":"ENSG00000104967"}}},"hgnc_date_symbol_changed":"1998-01-16"},"entity_type":"gene","entity_name":"NOVA2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber","PAGE DD-Gene2Phenotype"],"phenotypes":["Intellectual disability with ataxia/spasticity"],"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":["ANOVA"],"biotype":"protein_coding","hgnc_id":"HGNC:7887","gene_name":"NOVA alternative splicing regulator 2","omim_gene":["601991"],"alias_name":["neuro-oncological ventral antigen 3"],"gene_symbol":"NOVA2","hgnc_symbol":"NOVA2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:46436992-46476804","ensembl_id":"ENSG00000104967"}},"GRch38":{"90":{"location":"19:45933734-45973546","ensembl_id":"ENSG00000104967"}}},"hgnc_date_symbol_changed":"1998-01-16"},"entity_type":"gene","entity_name":"NOVA2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["DD-Gene2Phenotype","Expert Review Amber"],"phenotypes":["Intellectual disability with ataxia/spasticity"],"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"}]}}]}
