{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["AFURS1"],"biotype":"protein_coding","hgnc_id":"HGNC:24113","gene_name":"ATPase 13A3","omim_gene":["610232"],"alias_name":["ATPase family homolog up regulated in senescence cells"],"gene_symbol":"ATP13A3","hgnc_symbol":"ATP13A3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:194123401-194219093","ensembl_id":"ENSG00000133657"}},"GRch38":{"90":{"location":"3:194402672-194498364","ensembl_id":"ENSG00000133657"}}},"hgnc_date_symbol_changed":"2005-01-12"},"entity_type":"gene","entity_name":"ATP13A3","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["29650961","30545973"],"evidence":["NHS GMS","Expert Review Green","Literature"],"phenotypes":["Heritable pulmonary arterial hypertension","HPAH"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":193,"hash_id":"58c7f8a78f62033482c42716","name":"Pulmonary arterial hypertension","disease_group":"Cardiovascular disorders","disease_sub_group":"Pulmonary heart disease","status":"public","version":"2.0","version_created":"2019-09-23T17:04:36.560383Z","relevant_disorders":["PAH","R188"],"stats":{"number_of_genes":18,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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."}]}}]}