{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:16038","gene_name":"ORMDL sphingolipid biosynthesis regulator 3","omim_gene":["610075"],"alias_name":null,"gene_symbol":"ORMDL3","hgnc_symbol":"ORMDL3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:38077294-38083854","ensembl_id":"ENSG00000172057"}},"GRch38":{"90":{"location":"17:39921041-39927601","ensembl_id":"ENSG00000172057"}}},"hgnc_date_symbol_changed":"2001-07-27"},"entity_type":"gene","entity_name":"ORMDL3","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","NHS GMS"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":550,"hash_id":null,"name":"Respiratory ciliopathies including non-CF bronchiectasis","disease_group":"","disease_sub_group":"","status":"public","version":"0.156","version_created":"2019-09-27T18:48:31.875976Z","relevant_disorders":["R189"],"stats":{"number_of_genes":61,"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)"}]}}]}