{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["SAT-1","EDM4"],"biotype":"protein_coding","hgnc_id":"HGNC:10993","gene_name":"solute carrier family 26 member 1","omim_gene":["610130"],"alias_name":null,"gene_symbol":"SLC26A1","hgnc_symbol":"SLC26A1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:972861-987228","ensembl_id":"ENSG00000145217"}},"GRch38":{"90":{"location":"4:979073-993440","ensembl_id":"ENSG00000145217"}}},"hgnc_date_symbol_changed":"1999-07-30"},"entity_type":"gene","entity_name":"SLC26A1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Expert review red","Literature"],"phenotypes":["MIM 167030","Nephropathy of unknown origin","Nephrolithiasis calcium oxalate"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":720,"hash_id":null,"name":"Groopman et al 2019 - Genes with diagnostic variants","disease_group":"","disease_sub_group":"","status":"public","version":"0.8","version_created":"2019-07-09T15:48:14.145108Z","relevant_disorders":[],"stats":{"number_of_genes":66,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Submitted List","slug":"submitted-list","description":"Original list, ratings, comments submitted to PanelApp- generally used for the creation of reference GMS panels, these panels  should be internal only"}]}}]}