{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["NY-BR-85"],"biotype":"protein_coding","hgnc_id":"HGNC:25088","gene_name":"shugoshin 1","omim_gene":["609168"],"alias_name":null,"gene_symbol":"SGO1","hgnc_symbol":"SGO1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:20202085-20227784","ensembl_id":"ENSG00000129810"}},"GRch38":{"90":{"location":"3:20160593-20186292","ensembl_id":"ENSG00000129810"}}},"hgnc_date_symbol_changed":"2016-03-18"},"entity_type":"gene","entity_name":"SGO1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["25282101"],"evidence":["Expert Review Red","Other"],"phenotypes":["Chronic atrial and intestinal dysrhythmia 616201"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":["founder-effect"],"panel":{"id":61,"hash_id":"578e26918f62031b478bdb68","name":"Gastrointestinal neuromuscular disorders","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.10","version_created":"2018-12-16T17:39:16.981966Z","relevant_disorders":["Neonatal and familial gastrointestinal neuromuscular disorders","Infantile pseudo-obstruction","Early onset or familial intestinal pseudo obstruction"],"stats":{"number_of_genes":26,"number_of_strs":1,"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."}]}}]}