{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA1350"],"biotype":"protein_coding","hgnc_id":"HGNC:29255","gene_name":"ubiquitin specific peptidase 53","omim_gene":["617431"],"alias_name":null,"gene_symbol":"USP53","hgnc_symbol":"USP53","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:120133742-120216672","ensembl_id":"ENSG00000145390"}},"GRch38":{"90":{"location":"4:119212587-119295517","ensembl_id":"ENSG00000145390"}}},"hgnc_date_symbol_changed":"2004-01-28"},"entity_type":"gene","entity_name":"USP53","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["30250217"],"evidence":["Expert Review Amber","NHS GMS"],"phenotypes":["Paediatric cholestatic liver disease"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":544,"hash_id":null,"name":"Cholestasis","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-09-04T09:18:18.981248Z","relevant_disorders":["R171"],"stats":{"number_of_genes":39,"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)"},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}