{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["HUEL","ZNT9","GAC63"],"biotype":"protein_coding","hgnc_id":"HGNC:1329","gene_name":"solute carrier family 30 member 9","omim_gene":["604604"],"alias_name":["GRIP1-dependent nuclear receptor coactivator"],"gene_symbol":"SLC30A9","hgnc_symbol":"SLC30A9","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"4:41992489-42092474","ensembl_id":"ENSG00000014824"}},"GRch38":{"90":{"location":"4:41990472-42090457","ensembl_id":"ENSG00000014824"}}},"hgnc_date_symbol_changed":"2003-09-10"},"entity_type":"gene","entity_name":"SLC30A9","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["28334855"],"evidence":["Literature"],"phenotypes":["?Birk-Landau-Perez syndrome\t617595"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":285,"hash_id":"558aa423bb5a16630e15b63c","name":"Intellectual disability","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neurodevelopmental disorders","status":"public","version":"2.1065","version_created":"2019-10-07T13:42:16.019766Z","relevant_disorders":["Coarse facial features including Coffin-Siris-like disorders","ID","Moderate","severe or profound intellectual disability","Schizophrenia plus additional features","Intellectual disability - microarray","fragile X and sequencing"],"stats":{"number_of_genes":2253,"number_of_strs":11,"number_of_regions":57},"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."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}