{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MG1"],"biotype":"protein_coding","hgnc_id":"HGNC:7516","gene_name":"mucin 5B, oligomeric mucus/gel-forming","omim_gene":["600770"],"alias_name":null,"gene_symbol":"MUC5B","hgnc_symbol":"MUC5B","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"11:1244296-1283406","ensembl_id":"ENSG00000117983"}},"GRch38":{"90":{"location":"11:1223066-1262172","ensembl_id":"ENSG00000117983"}}},"hgnc_date_symbol_changed":"1991-12-03"},"entity_type":"gene","entity_name":"MUC5B","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["21506741"],"evidence":["Expert Review Red","Eligibility statement prior genetic testing","Radboud University Medical Center, Nijmegen"],"phenotypes":["{Pulmonary fibrosis, idiopathic, susceptibility to}, 178500"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":["promoter"],"panel":{"id":200,"hash_id":"563259de22c1fc58285b2840","name":"Familial pulmonary fibrosis","disease_group":"Respiratory disorders","disease_sub_group":"Interstitial lung disorders","status":"public","version":"1.6","version_created":"2019-08-20T14:18:14.336659Z","relevant_disorders":[],"stats":{"number_of_genes":71,"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."}]}}]}