{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["LRG47","LRG-47","IFI1"],"biotype":"protein_coding","hgnc_id":"HGNC:29597","gene_name":"immunity related GTPase M","omim_gene":["608212"],"alias_name":null,"gene_symbol":"IRGM","hgnc_symbol":"IRGM","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"5:150226085-150280298","ensembl_id":"ENSG00000237693"}},"GRch38":{"90":{"location":"5:150846523-150900736","ensembl_id":"ENSG00000237693"}}},"hgnc_date_symbol_changed":"2005-03-23"},"entity_type":"gene","entity_name":"IRGM","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":[],"evidence":["Other","Radboud University Medical Center, Nijmegen"],"phenotypes":["Inflammatory bowel disease 19, 612278","Crohn disease","{Inflammatory bowel disease (Crohn disease) 19}"],"mode_of_inheritance":"","tags":[],"panel":{"id":33,"hash_id":"56ba026422c1fc5025762b4f","name":"Gastrointestinal epithelial barrier disorders","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.59","version_created":"2019-06-20T15:11:44.535737Z","relevant_disorders":[],"stats":{"number_of_genes":82,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}