{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["IMP13","KIAA0724","RANBP13"],"biotype":"protein_coding","hgnc_id":"HGNC:16853","gene_name":"importin 13","omim_gene":["610411"],"alias_name":null,"gene_symbol":"IPO13","hgnc_symbol":"IPO13","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:44412611-44433694","ensembl_id":"ENSG00000117408"}},"GRch38":{"90":{"location":"1:43946939-43968022","ensembl_id":"ENSG00000117408"}}},"hgnc_date_symbol_changed":"2003-03-10"},"entity_type":"gene","entity_name":"IPO13","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["29700284"],"evidence":["Expert Review Amber","NHS GMS"],"phenotypes":[],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":509,"hash_id":null,"name":"Structural eye disease","disease_group":"","disease_sub_group":"","status":"public","version":"0.93","version_created":"2019-10-09T13:18:12.923145Z","relevant_disorders":["R36"],"stats":{"number_of_genes":456,"number_of_strs":0,"number_of_regions":2},"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)"}]}}]}