{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA1312"],"biotype":"protein_coding","hgnc_id":"HGNC:13202","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 9","omim_gene":["605421"],"alias_name":null,"gene_symbol":"ADAMTS9","hgnc_symbol":"ADAMTS9","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:64501333-64673676","ensembl_id":"ENSG00000163638"}},"GRch38":{"90":{"location":"3:64515654-64688000","ensembl_id":"ENSG00000163638"}}},"hgnc_date_symbol_changed":"2000-11-27"},"entity_type":"gene","entity_name":"ADAMTS9","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["30609407"],"evidence":["NHS GMS","Expert Review Amber"],"phenotypes":["Nephronophthisis-Related Ciliopathy (no OMIM number yet)"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":548,"hash_id":null,"name":"Tubulointerstitial kidney disease","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-09-03T13:37:53.887259Z","relevant_disorders":["R202"],"stats":{"number_of_genes":25,"number_of_strs":0,"number_of_regions":0},"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)"},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}},{"gene_data":{"alias":["KIAA1312"],"biotype":"protein_coding","hgnc_id":"HGNC:13202","gene_name":"ADAM metallopeptidase with thrombospondin type 1 motif 9","omim_gene":["605421"],"alias_name":null,"gene_symbol":"ADAMTS9","hgnc_symbol":"ADAMTS9","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:64501333-64673676","ensembl_id":"ENSG00000163638"}},"GRch38":{"90":{"location":"3:64515654-64688000","ensembl_id":"ENSG00000163638"}}},"hgnc_date_symbol_changed":"2000-11-27"},"entity_type":"gene","entity_name":"ADAMTS9","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"Other - please provide details in the comments","publications":["30609407"],"evidence":["Expert Review Amber","DD-Gene2Phenotype"],"phenotypes":["Nephronophthisis Related Ciliopathy"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"number_of_strs":0,"number_of_regions":0},"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)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}