{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ14600"],"biotype":"protein_coding","hgnc_id":"HGNC:25903","gene_name":"ATPase family, AAA domain containing 1","omim_gene":["614452"],"alias_name":["thorase"],"gene_symbol":"ATAD1","hgnc_symbol":"ATAD1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"10:89511269-89601100","ensembl_id":"ENSG00000138138"}},"GRch38":{"90":{"location":"10:87751512-87841343","ensembl_id":"ENSG00000138138"}}},"hgnc_date_symbol_changed":"2007-02-08"},"entity_type":"gene","entity_name":"ATAD1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Green","NHS GMS","Wessex and West Midlands GLH"],"phenotypes":["Hyperekplexia 4, 618011"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":541,"hash_id":null,"name":"Paroxysmal central nervous system disorders","disease_group":"","disease_sub_group":"","status":"public","version":"0.168","version_created":"2019-10-01T13:39:46.962209Z","relevant_disorders":["Paroxysmal neurological disorders","pain disorders and sleep disorders"],"stats":{"number_of_genes":83,"number_of_strs":5,"number_of_regions":1},"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)"}]}}]}