{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["bHLHc8"],"biotype":"protein_coding","hgnc_id":"HGNC:24669","gene_name":"folliculogenesis specific bHLH transcription factor","omim_gene":["608697"],"alias_name":["factor in the germline alpha"],"gene_symbol":"FIGLA","hgnc_symbol":"FIGLA","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"2:71004442-71017775","ensembl_id":"ENSG00000183733"}},"GRch38":{"90":{"location":"2:70777310-70790643","ensembl_id":"ENSG00000183733"}}},"hgnc_date_symbol_changed":"2006-05-18"},"entity_type":"gene","entity_name":"FIGLA","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["18499083"],"evidence":["Expert Review Amber","Other","Illumina TruGenome Clinical Sequencing Services","Radboud University Medical Center, Nijmegen"],"phenotypes":["Premature ovarian failure,612310","Premature Ovarian Failure"],"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."}]}}]}