{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["VGR1"],"biotype":"protein_coding","hgnc_id":"HGNC:1073","gene_name":"bone morphogenetic protein 6","omim_gene":["112266"],"alias_name":null,"gene_symbol":"BMP6","hgnc_symbol":"BMP6","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:7727030-7881655","ensembl_id":"ENSG00000153162"}},"GRch38":{"90":{"location":"6:7726797-7881422","ensembl_id":"ENSG00000153162"}}},"hgnc_date_symbol_changed":"1991-06-05"},"entity_type":"gene","entity_name":"BMP6","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["26582087"],"evidence":["North West GLH","Yorkshire and North East GLH","London South GLH","NHS GMS","Expert Review Green","Wessex and West Midlands GLH"],"phenotypes":["NA IRON OVERLOAD","112266 Mild to moderate iron overload","Iron overload"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":515,"hash_id":null,"name":"Iron metabolism disorders","disease_group":"","disease_sub_group":"","status":"public","version":"1.1","version_created":"2019-09-23T14:47:26.293257Z","relevant_disorders":["R96"],"stats":{"number_of_genes":26,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}