{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MGC12372"],"biotype":"protein_coding","hgnc_id":"HGNC:4026","gene_name":"FXYD domain containing ion transport regulator 2","omim_gene":["601814"],"alias_name":null,"gene_symbol":"FXYD2","hgnc_symbol":"FXYD2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"11:117671559-117699413","ensembl_id":"ENSG00000137731"}},"GRch38":{"90":{"location":"11:117800844-117828698","ensembl_id":"ENSG00000137731"}}},"hgnc_date_symbol_changed":"1997-06-12"},"entity_type":"gene","entity_name":"FXYD2","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27604308"],"evidence":["Expert Review Red","Literature"],"phenotypes":["Hypomagnesaemia type 2, renal (Disorder of magnesium metabolism)","Hypomagnesemia 2, renal  154020"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":["founder-effect"],"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":["MGC12372"],"biotype":"protein_coding","hgnc_id":"HGNC:4026","gene_name":"FXYD domain containing ion transport regulator 2","omim_gene":["601814"],"alias_name":null,"gene_symbol":"FXYD2","hgnc_symbol":"FXYD2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"11:117671559-117699413","ensembl_id":"ENSG00000137731"}},"GRch38":{"90":{"location":"11:117800844-117828698","ensembl_id":"ENSG00000137731"}}},"hgnc_date_symbol_changed":"1997-06-12"},"entity_type":"gene","entity_name":"FXYD2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["27604308"],"evidence":["London North GLH","NHS GMS","Expert Review Red"],"phenotypes":["Hypomagnesemia 2, renal  154020","Hypomagnesaemia type 2, renal (Disorder of magnesium metabolism)"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status 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"}]}},{"gene_data":{"alias":["MGC12372"],"biotype":"protein_coding","hgnc_id":"HGNC:4026","gene_name":"FXYD domain containing ion transport regulator 2","omim_gene":["601814"],"alias_name":null,"gene_symbol":"FXYD2","hgnc_symbol":"FXYD2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"11:117671559-117699413","ensembl_id":"ENSG00000137731"}},"GRch38":{"90":{"location":"11:117800844-117828698","ensembl_id":"ENSG00000137731"}}},"hgnc_date_symbol_changed":"1997-06-12"},"entity_type":"gene","entity_name":"FXYD2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["11062458","25765846"],"evidence":["Expert Review Amber","NHS GMS"],"phenotypes":["Hypomagnesemia 2, renal, 154020"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":292,"hash_id":"553f94d5bb5a1616e5ed45a4","name":"Renal tubulopathies","disease_group":"Renal and urinary tract disorders","disease_sub_group":"Disorders of function","status":"public","version":"1.193","version_created":"2019-10-09T09:34:39.432250Z","relevant_disorders":["Renal tubular acidosis","R198"],"stats":{"number_of_genes":55,"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)"}]}}]}