{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["C6.1A","BRCC36"],"biotype":"protein_coding","hgnc_id":"HGNC:24185","gene_name":"BRCA1/BRCA2-containing complex subunit 3","omim_gene":["300617"],"alias_name":["Lys-63-specific deubiquitinase"],"gene_symbol":"BRCC3","hgnc_symbol":"BRCC3","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"X:154299695-154351349","ensembl_id":"ENSG00000185515"}},"GRch38":{"90":{"location":"X:155071420-155123074","ensembl_id":"ENSG00000185515"}}},"hgnc_date_symbol_changed":"2005-11-21"},"entity_type":"gene","entity_name":"BRCC3","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["21596366"],"evidence":["Expert Review Red","Expert list"],"phenotypes":["Moyamoya disease"],"mode_of_inheritance":"X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","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."}]}}]}