{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MMSET","KMT3G"],"biotype":"protein_coding","hgnc_id":"HGNC:12766","gene_name":"nuclear receptor binding SET domain protein 2","omim_gene":["602952"],"alias_name":["multiple myeloma SET domain containing protein"],"gene_symbol":"NSD2","hgnc_symbol":"NSD2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:1873151-1983934","ensembl_id":"ENSG00000109685"}},"GRch38":{"90":{"location":"4:1871424-1982207","ensembl_id":"ENSG00000109685"}}},"hgnc_date_symbol_changed":"2016-11-18"},"entity_type":"gene","entity_name":"NSD2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","NHS GMS"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":549,"hash_id":null,"name":"Laterality disorders and isomerism","disease_group":"","disease_sub_group":"","status":"public","version":"0.51","version_created":"2019-09-27T19:31:06.459183Z","relevant_disorders":["R139"],"stats":{"number_of_genes":56,"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)"}]}},{"gene_data":{"alias":["MMSET","KMT3G"],"biotype":"protein_coding","hgnc_id":"HGNC:12766","gene_name":"nuclear receptor binding SET domain protein 2","omim_gene":["602952"],"alias_name":["multiple myeloma SET domain containing protein"],"gene_symbol":"NSD2","hgnc_symbol":"NSD2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:1873151-1983934","ensembl_id":"ENSG00000109685"}},"GRch38":{"90":{"location":"4:1871424-1982207","ensembl_id":"ENSG00000109685"}}},"hgnc_date_symbol_changed":"2016-11-18"},"entity_type":"gene","entity_name":"NSD2","confidence_level":"3","penetrance":"unknown","mode_of_pathogenicity":null,"publications":["29892088","29760529","29884796","30244530"],"evidence":["Expert Review Green","Expert Review","Literature"],"phenotypes":["Intrauterine growth retardation","Growth delay","Microcephaly","Muscular hypotonia","Neurodevelopmental delay","Intellectual disability","No OMIM number"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","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"}]}}]}