{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:12382","gene_name":"TSPY like 1","omim_gene":["604714"],"alias_name":null,"gene_symbol":"TSPYL1","hgnc_symbol":"TSPYL1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"6:116597741-116601066","ensembl_id":"ENSG00000189241"}},"GRch38":{"90":{"location":"6:116276578-116279903","ensembl_id":"ENSG00000189241"}}},"hgnc_date_symbol_changed":"2004-04-07"},"entity_type":"gene","entity_name":"TSPYL1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Other","Radboud University Medical Center, Nijmegen"],"phenotypes":["Sudden infant death with dysgenesis of the testes syndrome,608800","SIDDT"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":["founder-effect"],"panel":{"id":45,"hash_id":"5763f6508f620350a1996055","name":"Sudden death in young people","disease_group":"Cardiovascular disorders","disease_sub_group":"Cardiac arrhythmia","status":"public","version":"1.12","version_created":"2019-06-20T15:15:17.414434Z","relevant_disorders":["Unexplained sudden death in the young"],"stats":{"number_of_genes":35,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:12382","gene_name":"TSPY like 1","omim_gene":["604714"],"alias_name":null,"gene_symbol":"TSPYL1","hgnc_symbol":"TSPYL1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"6:116597741-116601066","ensembl_id":"ENSG00000189241"}},"GRch38":{"90":{"location":"6:116276578-116279903","ensembl_id":"ENSG00000189241"}}},"hgnc_date_symbol_changed":"2004-04-07"},"entity_type":"gene","entity_name":"TSPYL1","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["15273283","22137496","19463995"],"evidence":["Expert Review Amber","Other","Radboud University Medical Center, Nijmegen","Expert list"],"phenotypes":["Sudden infant death with dysgenesis of the testes syndrome\t608800"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":9,"hash_id":"569380ac22c1fc251660faf8","name":"Disorders of sex development","disease_group":"Endocrine disorders","disease_sub_group":"Gonadal and sex development disorders","status":"public","version":"2.1","version_created":"2019-10-01T10:16:03.440399Z","relevant_disorders":["R146"],"stats":{"number_of_genes":54,"number_of_strs":0,"number_of_regions":1},"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."},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}