{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:6344","gene_name":"klotho","omim_gene":["604824"],"alias_name":null,"gene_symbol":"KL","hgnc_symbol":"KL","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"13:33590207-33640282","ensembl_id":"ENSG00000133116"}},"GRch38":{"90":{"location":"13:33016433-33066145","ensembl_id":"ENSG00000133116"}}},"hgnc_date_symbol_changed":"1999-03-24"},"entity_type":"gene","entity_name":"KL","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["17710231"],"evidence":["NHS GMS"],"phenotypes":["Tumoral calcinosis, hyperphosphatemic, familial, 3 617994"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":552,"hash_id":null,"name":"Familial tumoral calcinosis","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-07-31T14:36:02.985916Z","relevant_disorders":["R162"],"stats":{"number_of_genes":4,"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."}]}}]}