{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["JJAZ1","KIAA0160","CHET9"],"biotype":"protein_coding","hgnc_id":"HGNC:17101","gene_name":"SUZ12 polycomb repressive complex 2 subunit","omim_gene":["606245"],"alias_name":null,"gene_symbol":"SUZ12","hgnc_symbol":"SUZ12","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:30264037-30328064","ensembl_id":"ENSG00000178691"}},"GRch38":{"90":{"location":"17:31937018-32001045","ensembl_id":"ENSG00000178691"}}},"hgnc_date_symbol_changed":"2004-12-14"},"entity_type":"gene","entity_name":"SUZ12","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["30019515","28229514"],"evidence":["Expert Review Green","DD-Gene2Phenotype"],"phenotypes":["Weaver-like overgrowth syndrome"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":478,"hash_id":null,"name":"Fetal anomalies","disease_group":"","disease_sub_group":"","status":"public","version":"0.344","version_created":"2019-09-17T09:38:10.568007Z","relevant_disorders":["R21"],"stats":{"number_of_genes":1721,"number_of_strs":0,"number_of_regions":0},"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."}]}},{"gene_data":{"alias":["JJAZ1","KIAA0160","CHET9"],"biotype":"protein_coding","hgnc_id":"HGNC:17101","gene_name":"SUZ12 polycomb repressive complex 2 subunit","omim_gene":["606245"],"alias_name":null,"gene_symbol":"SUZ12","hgnc_symbol":"SUZ12","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:30264037-30328064","ensembl_id":"ENSG00000178691"}},"GRch38":{"90":{"location":"17:31937018-32001045","ensembl_id":"ENSG00000178691"}}},"hgnc_date_symbol_changed":"2004-12-14"},"entity_type":"gene","entity_name":"SUZ12","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["30019515","28229514"],"evidence":["Expert Review Green","DD-Gene2Phenotype"],"phenotypes":["Weaver-like overgrowth syndrome"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","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"}]}}]}