{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CREB-H"],"biotype":"protein_coding","hgnc_id":"HGNC:18855","gene_name":"cAMP responsive element binding protein 3 like 3","omim_gene":["611998"],"alias_name":null,"gene_symbol":"CREB3L3","hgnc_symbol":"CREB3L3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:4153598-4173051","ensembl_id":"ENSG00000060566"}},"GRch38":{"90":{"location":"19:4153601-4173054","ensembl_id":"ENSG00000060566"}}},"hgnc_date_symbol_changed":"2003-12-09"},"entity_type":"gene","entity_name":"CREB3L3","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["29954705","21666694","26427795","22135386"],"evidence":["Expert Review Green","Literature"],"phenotypes":["monogenic dominant hypertriglyceridemia associated with CREB3L3"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":228,"hash_id":"57eab3658f620356ef5e4010","name":"Severe hypertriglyceridaemia","disease_group":"Cardiovascular disorders","disease_sub_group":"Arteriopathies","status":"public","version":"1.12","version_created":"2019-07-23T11:06:24.015746Z","relevant_disorders":[],"stats":{"number_of_genes":8,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["CREB-H"],"biotype":"protein_coding","hgnc_id":"HGNC:18855","gene_name":"cAMP responsive element binding protein 3 like 3","omim_gene":["611998"],"alias_name":null,"gene_symbol":"CREB3L3","hgnc_symbol":"CREB3L3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:4153598-4173051","ensembl_id":"ENSG00000060566"}},"GRch38":{"90":{"location":"19:4153601-4173054","ensembl_id":"ENSG00000060566"}}},"hgnc_date_symbol_changed":"2003-12-09"},"entity_type":"gene","entity_name":"CREB3L3","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["29954705","21666694","26427795","22135386"],"evidence":["Expert Review Green","South West GLH","NHS GMS"],"phenotypes":["monogenic dominant hypertriglyceridemia associated with CREB3L3"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":527,"hash_id":null,"name":"Lipoprotein lipase deficiency","disease_group":"","disease_sub_group":"","status":"public","version":"1.0","version_created":"2019-08-13T10:58:13.987962Z","relevant_disorders":["R324"],"stats":{"number_of_genes":10,"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."}]}}]}
