{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["4E-T","FLJ21601","Clast4","2610509L04Rik"],"biotype":"protein_coding","hgnc_id":"HGNC:16687","gene_name":"eukaryotic translation initiation factor 4E nuclear import factor 1","omim_gene":["607445"],"alias_name":null,"gene_symbol":"EIF4ENIF1","hgnc_symbol":"EIF4ENIF1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"22:31832963-31892094","ensembl_id":"ENSG00000184708"}},"GRch38":{"90":{"location":"22:31436977-31496108","ensembl_id":"ENSG00000184708"}}},"hgnc_date_symbol_changed":"2002-06-18"},"entity_type":"gene","entity_name":"EIF4ENIF1","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["23902945"],"evidence":["Literature","Expert Review Amber","Expert list"],"phenotypes":["premature ovarian failure","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."}]}}]}