{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["ECNOS","eNOS"],"biotype":"protein_coding","hgnc_id":"HGNC:7876","gene_name":"nitric oxide synthase 3","omim_gene":["163729"],"alias_name":["endothelial nitric oxide synthase"],"gene_symbol":"NOS3","hgnc_symbol":"NOS3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:150688083-150711676","ensembl_id":"ENSG00000164867"}},"GRch38":{"90":{"location":"7:150990995-151014588","ensembl_id":"ENSG00000164867"}}},"hgnc_date_symbol_changed":"1993-08-23"},"entity_type":"gene","entity_name":"NOS3","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["28787010"],"evidence":["Literature"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":394,"hash_id":null,"name":"Familial Meniere Disease","disease_group":"Hearing and ear disorders","disease_sub_group":"Other hearing and ear disorders","status":"public","version":"1.1","version_created":"2018-01-17T16:26:29.432517Z","relevant_disorders":[],"stats":{"number_of_genes":130,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}