{"count":5,"next":null,"previous":null,"results":[{"gene_data":{"alias":["Glut9","GLUTX","URATv1"],"biotype":"protein_coding","hgnc_id":"HGNC:13446","gene_name":"solute carrier family 2 member 9","omim_gene":["606142"],"alias_name":["urate voltage-driven efflux transporter 1"],"gene_symbol":"SLC2A9","hgnc_symbol":"SLC2A9","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"4:9772777-10056560","ensembl_id":"ENSG00000109667"}},"GRch38":{"90":{"location":"4:9771153-10054936","ensembl_id":"ENSG00000109667"}}},"hgnc_date_symbol_changed":"2000-09-28"},"entity_type":"gene","entity_name":"SLC2A9","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Expert Review"],"phenotypes":["Hypouricemia, renal, 2\t612076","{Uric acid concentration, serum, QTL 2}\t612076"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","tags":[],"panel":{"id":66,"hash_id":"55b63d7f22c1fc05fc7a185b","name":"Rhabdomyolysis and metabolic muscle disorders","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neuromuscular disorders","status":"public","version":"1.28","version_created":"2019-08-08T11:47:51.945935Z","relevant_disorders":[],"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 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."}]}},{"gene_data":{"alias":["Glut9","GLUTX","URATv1"],"biotype":"protein_coding","hgnc_id":"HGNC:13446","gene_name":"solute carrier family 2 member 9","omim_gene":["606142"],"alias_name":["urate voltage-driven efflux transporter 1"],"gene_symbol":"SLC2A9","hgnc_symbol":"SLC2A9","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:9772777-10056560","ensembl_id":"ENSG00000109667"}},"GRch38":{"90":{"location":"4:9771153-10054936","ensembl_id":"ENSG00000109667"}}},"hgnc_date_symbol_changed":"2000-09-28"},"entity_type":"gene","entity_name":"SLC2A9","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red"],"phenotypes":["Hypouricemia, renal, 2"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","tags":[],"panel":{"id":465,"hash_id":null,"name":"Neuromuscular disorders","disease_group":"","disease_sub_group":"","status":"public","version":"1.11","version_created":"2019-10-09T12:42:27.875560Z","relevant_disorders":["Other rare neuromuscular disorders; R381"],"stats":{"number_of_genes":245,"number_of_strs":2,"number_of_regions":5},"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":["Glut9","GLUTX","URATv1"],"biotype":"protein_coding","hgnc_id":"HGNC:13446","gene_name":"solute carrier family 2 member 9","omim_gene":["606142"],"alias_name":["urate voltage-driven efflux transporter 1"],"gene_symbol":"SLC2A9","hgnc_symbol":"SLC2A9","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"4:9772777-10056560","ensembl_id":"ENSG00000109667"}},"GRch38":{"90":{"location":"4:9771153-10054936","ensembl_id":"ENSG00000109667"}}},"hgnc_date_symbol_changed":"2000-09-28"},"entity_type":"gene","entity_name":"SLC2A9","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert"],"phenotypes":[],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","tags":[],"panel":{"id":149,"hash_id":"553f94d5bb5a1616e5ed45a5","name":"Nephrocalcinosis or nephrolithiasis","disease_group":"Renal and urinary tract disorders","disease_sub_group":"Disorders of function","status":"public","version":"1.18","version_created":"2019-09-17T20:55:27.132282Z","relevant_disorders":["Renal tract calcification (or Nephrolithiasis or nephrocalcinosis)","Renal tract calcification (or Nephrolithiasis/nephrocalcinosis)","R256"],"stats":{"number_of_genes":42,"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)"}]}},{"gene_data":{"alias":["Glut9","GLUTX","URATv1"],"biotype":"protein_coding","hgnc_id":"HGNC:13446","gene_name":"solute carrier family 2 member 9","omim_gene":["606142"],"alias_name":["urate voltage-driven efflux transporter 1"],"gene_symbol":"SLC2A9","hgnc_symbol":"SLC2A9","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:9772777-10056560","ensembl_id":"ENSG00000109667"}},"GRch38":{"90":{"location":"4:9771153-10054936","ensembl_id":"ENSG00000109667"}}},"hgnc_date_symbol_changed":"2000-09-28"},"entity_type":"gene","entity_name":"SLC2A9","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["19026395","19926891","21810765"],"evidence":["Expert Review Green","NHS GMS"],"phenotypes":["{Uric acid concentration, serum, QTL 2}, 612076","Hypouricemia, renal, 2, 612076"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","tags":[],"panel":{"id":678,"hash_id":null,"name":"Unexplained paediatric onset end-stage renal disease","disease_group":"","disease_sub_group":"","status":"public","version":"0.43","version_created":"2019-09-25T12:25:36.245604Z","relevant_disorders":["R257"],"stats":{"number_of_genes":229,"number_of_strs":0,"number_of_regions":3},"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)"}]}},{"gene_data":{"alias":["Glut9","GLUTX","URATv1"],"biotype":"protein_coding","hgnc_id":"HGNC:13446","gene_name":"solute carrier family 2 member 9","omim_gene":["606142"],"alias_name":["urate voltage-driven efflux transporter 1"],"gene_symbol":"SLC2A9","hgnc_symbol":"SLC2A9","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:9772777-10056560","ensembl_id":"ENSG00000109667"}},"GRch38":{"90":{"location":"4:9771153-10054936","ensembl_id":"ENSG00000109667"}}},"hgnc_date_symbol_changed":"2000-09-28"},"entity_type":"gene","entity_name":"SLC2A9","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["19026395","19926891","21810765"],"evidence":["Expert Review Green","NHS GMS"],"phenotypes":["Hypouricemia, renal, 2, 612076","{Uric acid concentration, serum, QTL 2}, 612076"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","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)"}]}}]}