{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA1554","NET57"],"biotype":"protein_coding","hgnc_id":"HGNC:14539","gene_name":"ring finger protein 213","omim_gene":["613768"],"alias_name":null,"gene_symbol":"RNF213","hgnc_symbol":"RNF213","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"17:78234665-78372586","ensembl_id":"ENSG00000173821"}},"GRch38":{"90":{"location":"17:80260866-80398786","ensembl_id":"ENSG00000173821"}}},"hgnc_date_symbol_changed":"2007-02-08"},"entity_type":"gene","entity_name":"RNF213","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Expert list","Other"],"phenotypes":["{Moyamoya disease 2, susceptibility to}"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":147,"hash_id":"5819a24f8f6203341de99c89","name":"Cerebral vascular malformations","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Cerebrovascular disorders","status":"public","version":"1.47","version_created":"2019-09-13T13:47:21.970257Z","relevant_disorders":["Cerebrovascular disorders","Vein of Galen malformation","Cerebral arteriovenous malformations","Moyamoya disease"],"stats":{"number_of_genes":95,"number_of_strs":0,"number_of_regions":0},"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."}]}}]}