{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["OPLA","5-Opase"],"biotype":"protein_coding","hgnc_id":"HGNC:8149","gene_name":"5-oxoprolinase, ATP-hydrolysing","omim_gene":["614243"],"alias_name":null,"gene_symbol":"OPLAH","hgnc_symbol":"OPLAH","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"8:145106167-145118735","ensembl_id":"ENSG00000178814"}},"GRch38":{"90":{"location":"8:144051266-144063965","ensembl_id":"ENSG00000178814"}}},"hgnc_date_symbol_changed":"1999-12-10"},"entity_type":"gene","entity_name":"OPLAH","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27604308","21651516","23430506","27477828"],"evidence":["Expert Review Amber","Radboud University Medical Center, Nijmegen","Literature"],"phenotypes":["5-oxoprolinase deficiency 260005"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","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":["OPLA","5-Opase"],"biotype":"protein_coding","hgnc_id":"HGNC:8149","gene_name":"5-oxoprolinase, ATP-hydrolysing","omim_gene":["614243"],"alias_name":null,"gene_symbol":"OPLAH","hgnc_symbol":"OPLAH","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"8:145106167-145118735","ensembl_id":"ENSG00000178814"}},"GRch38":{"90":{"location":"8:144051266-144063965","ensembl_id":"ENSG00000178814"}}},"hgnc_date_symbol_changed":"1999-12-10"},"entity_type":"gene","entity_name":"OPLAH","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["27604308","21651516","23430506","27477828"],"evidence":["Expert Review Amber","London North GLH","NHS GMS"],"phenotypes":["5-oxoprolinase deficiency 260005"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","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"}]}}]}
