{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FSHRO","LGR1"],"biotype":"protein_coding","hgnc_id":"HGNC:3969","gene_name":"follicle stimulating hormone receptor","omim_gene":["136435"],"alias_name":null,"gene_symbol":"FSHR","hgnc_symbol":"FSHR","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"2:49189296-49381676","ensembl_id":"ENSG00000170820"}},"GRch38":{"90":{"location":"2:48962157-49154537","ensembl_id":"ENSG00000170820"}}},"hgnc_date_symbol_changed":"1991-07-09"},"entity_type":"gene","entity_name":"FSHR","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Green","Other","Illumina TruGenome Clinical Sequencing Services","Radboud University Medical Center, Nijmegen"],"phenotypes":["Ovarian dysgenesis 1\t233300","Ovarian response to FSH stimulation\t276400"],"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."}]}}]}