{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:399","gene_name":"albumin","omim_gene":["103600"],"alias_name":null,"gene_symbol":"ALB","hgnc_symbol":"ALB","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:74262831-74287129","ensembl_id":"ENSG00000163631"}},"GRch38":{"90":{"location":"4:73397114-73421412","ensembl_id":"ENSG00000163631"}}},"hgnc_date_symbol_changed":"2006-06-30"},"entity_type":"gene","entity_name":"ALB","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["29163366","8064810","24646103","27834068"],"evidence":["Expert Review Green","Expert list"],"phenotypes":["Familial dysalbuminaemic hyperthyroxinaemia","[Dysalbuminemic hyperthyroxinemia], 615999"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":236,"hash_id":"576cd44c8f6203609632be80","name":"Hyperthyroidism","disease_group":"Endocrine disorders","disease_sub_group":"Thyroid disorders","status":"public","version":"2.0","version_created":"2019-07-31T15:03:48.384099Z","relevant_disorders":["Resistance to thyroid hormone","R182"],"stats":{"number_of_genes":7,"number_of_strs":0,"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."},{"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."}]}}]}