{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FTH","PLIF","PIG15","FHC"],"biotype":"protein_coding","hgnc_id":"HGNC:3976","gene_name":"ferritin heavy chain 1","omim_gene":["134770"],"alias_name":["apoferritin","placenta immunoregulatory factor","proliferation-inducing protein 15"],"gene_symbol":"FTH1","hgnc_symbol":"FTH1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"11:61727190-61735132","ensembl_id":"ENSG00000167996"}},"GRch38":{"90":{"location":"11:61959718-61967660","ensembl_id":"ENSG00000167996"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"FTH1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["11389486"],"evidence":["Expert Review Amber","North West GLH","Yorkshire and North East GLH","London South GLH","NHS GMS","Wessex and West Midlands GLH"],"phenotypes":["615517 ?Hemochromatosis, type 5","HFE5","615517 HEMOCHROMATOSIS, TYPE 5"],"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."}]}}]}