{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PTP18","RPTPB","phosphacan"],"biotype":"protein_coding","hgnc_id":"HGNC:9685","gene_name":"protein tyrosine phosphatase, receptor type Z1","omim_gene":["176891"],"alias_name":null,"gene_symbol":"PTPRZ1","hgnc_symbol":"PTPRZ1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"7:121513143-121702090","ensembl_id":"ENSG00000106278"}},"GRch38":{"90":{"location":"7:121873089-122062036","ensembl_id":"ENSG00000106278"}}},"hgnc_date_symbol_changed":"1991-05-15"},"entity_type":"gene","entity_name":"PTPRZ1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27604308"],"evidence":["Expert Review Red","Literature"],"phenotypes":["Hyperlysinaemia (Disorders of histidine, tryptophan or lysine metabolism)","{H. pylori infection, susceptibility to} 600263"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":302,"hash_id":"5763f1518f620350a22bccdb","name":"Undiagnosed metabolic disorders","disease_group":"Metabolic disorders","disease_sub_group":"Specific metabolic abnormalities","status":"public","version":"1.373","version_created":"2019-10-08T14:47:17.153678Z","relevant_disorders":["Undiagnosed Metabolic Panel"],"stats":{"number_of_genes":744,"number_of_strs":1,"number_of_regions":1},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["PTP18","RPTPB","phosphacan"],"biotype":"protein_coding","hgnc_id":"HGNC:9685","gene_name":"protein tyrosine phosphatase, receptor type Z1","omim_gene":["176891"],"alias_name":null,"gene_symbol":"PTPRZ1","hgnc_symbol":"PTPRZ1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:121513143-121702090","ensembl_id":"ENSG00000106278"}},"GRch38":{"90":{"location":"7:121873089-122062036","ensembl_id":"ENSG00000106278"}}},"hgnc_date_symbol_changed":"1991-05-15"},"entity_type":"gene","entity_name":"PTPRZ1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["27604308"],"evidence":["London North GLH","NHS GMS","Expert Review Red"],"phenotypes":["Hyperlysinaemia (Disorders of histidine, tryptophan or lysine metabolism)","{H. pylori infection, susceptibility to} 600263"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":467,"hash_id":null,"name":"Inborn errors of metabolism","disease_group":"","disease_sub_group":"","status":"public","version":"1.348","version_created":"2019-10-09T08:19:52.386941Z","relevant_disorders":["Likely inborn error of metabolism - targeted testing not possible"],"stats":{"number_of_genes":877,"number_of_strs":2,"number_of_regions":1},"types":[{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}
