{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MKP-3","PYST1"],"biotype":"protein_coding","hgnc_id":"HGNC:3072","gene_name":"dual specificity phosphatase 6","omim_gene":["602748"],"alias_name":null,"gene_symbol":"DUSP6","hgnc_symbol":"DUSP6","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"12:89741009-89747048","ensembl_id":"ENSG00000139318"}},"GRch38":{"90":{"location":"12:89347232-89353271","ensembl_id":"ENSG00000139318"}}},"hgnc_date_symbol_changed":"1997-03-19"},"entity_type":"gene","entity_name":"DUSP6","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["23643382"],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen","OMIM"],"phenotypes":["Hypogonadotropic hypogonadism 19 with or without anosmia, 615269"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":["monogenic-polygenic"],"panel":{"id":92,"hash_id":"573b204d8f62030defb98057","name":"Hypogonadotropic hypogonadism","disease_group":"Endocrine disorders","disease_sub_group":"Hypothalamic and pituitary disorders","status":"public","version":"1.26","version_created":"2019-06-20T15:11:57.281996Z","relevant_disorders":["Kallmann syndrome","Kallmann syndrom","Idiopathic hypogonadotropic hypogonadism"],"stats":{"number_of_genes":46,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["MKP-3","PYST1"],"biotype":"protein_coding","hgnc_id":"HGNC:3072","gene_name":"dual specificity phosphatase 6","omim_gene":["602748"],"alias_name":null,"gene_symbol":"DUSP6","hgnc_symbol":"DUSP6","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"12:89741009-89747048","ensembl_id":"ENSG00000139318"}},"GRch38":{"90":{"location":"12:89347232-89353271","ensembl_id":"ENSG00000139318"}}},"hgnc_date_symbol_changed":"1997-03-19"},"entity_type":"gene","entity_name":"DUSP6","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","PAGE Additional Gene List"],"phenotypes":["Hypogonadotropic hypogonadism 19 with or without anosmia 615269"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":478,"hash_id":null,"name":"Fetal anomalies","disease_group":"","disease_sub_group":"","status":"public","version":"0.344","version_created":"2019-09-17T09:38:10.568007Z","relevant_disorders":["R21"],"stats":{"number_of_genes":1721,"number_of_strs":0,"number_of_regions":0},"types":[{"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."}]}}]}