{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["TRIPIN","FLJ25211"],"biotype":"protein_coding","hgnc_id":"HGNC:30812","gene_name":"shugoshin 2","omim_gene":["612425"],"alias_name":null,"gene_symbol":"SGO2","hgnc_symbol":"SGO2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"2:201374731-201448505","ensembl_id":"ENSG00000163535"}},"GRch38":{"90":{"location":"2:200510008-200583782","ensembl_id":"ENSG00000163535"}}},"hgnc_date_symbol_changed":"2016-03-18"},"entity_type":"gene","entity_name":"SGO2","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27629923"],"evidence":["Expert Review Amber","Literature"],"phenotypes":["PERRAULT SYNDROME"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":155,"hash_id":"575ed2398f62034208b69ee1","name":"Primary ovarian insufficiency","disease_group":"Endocrine disorders","disease_sub_group":"Gonadal and sex development disorders","status":"public","version":"1.16","version_created":"2019-06-20T15:13:53.581309Z","relevant_disorders":["Early onset familial premature ovarian insufficiency","Early onset familial premature ovarian failure"],"stats":{"number_of_genes":56,"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."}]}}]}