{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ20449","TEB1","bHLHe81","SPATA28"],"biotype":"protein_coding","hgnc_id":"HGNC:26026","gene_name":"spermatogenesis and oogenesis specific basic helix-loop-helix 2","omim_gene":["616066"],"alias_name":["spermatogenesis associated 28"],"gene_symbol":"SOHLH2","hgnc_symbol":"SOHLH2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"13:36742345-36871979","ensembl_id":"ENSG00000120669"}},"GRch38":{"90":{"location":"13:36168208-36214615","ensembl_id":"ENSG00000120669"}}},"hgnc_date_symbol_changed":"2006-03-16"},"entity_type":"gene","entity_name":"SOHLH2","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["24524832"],"evidence":["Expert Review Amber","Literature"],"phenotypes":["Primary ovarian insufficiency"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","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."}]}}]}