{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MEL1","PFM13","KIAA1675","MGC166915","KMT8F"],"biotype":"protein_coding","hgnc_id":"HGNC:14000","gene_name":"PR/SET domain 16","omim_gene":["605557"],"alias_name":["MDS1/EVI1-like","PR-domain zinc finger protein 16","transcription factor MEL1"],"gene_symbol":"PRDM16","hgnc_symbol":"PRDM16","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:2985732-3355185","ensembl_id":"ENSG00000142611"}},"GRch38":{"90":{"location":"1:3069168-3438621","ensembl_id":"ENSG00000142611"}}},"hgnc_date_symbol_changed":"2000-11-28"},"entity_type":"gene","entity_name":"PRDM16","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["Left ventricular noncompaction 8"],"mode_of_inheritance":"","tags":[],"panel":{"id":238,"hash_id":"55a38d3a22c1fc64c2942434","name":"Left Ventricular Noncompaction Cardiomyopathy","disease_group":"Cardiovascular disorders","disease_sub_group":"Cardiomyopathy","status":"public","version":"1.3","version_created":"2019-06-20T15:15:12.623782Z","relevant_disorders":[],"stats":{"number_of_genes":16,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["MEL1","PFM13","KIAA1675","MGC166915","KMT8F"],"biotype":"protein_coding","hgnc_id":"HGNC:14000","gene_name":"PR/SET domain 16","omim_gene":["605557"],"alias_name":["MDS1/EVI1-like","PR-domain zinc finger protein 16","transcription factor MEL1"],"gene_symbol":"PRDM16","hgnc_symbol":"PRDM16","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:2985732-3355185","ensembl_id":"ENSG00000142611"}},"GRch38":{"90":{"location":"1:3069168-3438621","ensembl_id":"ENSG00000142611"}}},"hgnc_date_symbol_changed":"2000-11-28"},"entity_type":"gene","entity_name":"PRDM16","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["South West GLH","London South GLH","Radboud University Medical Center, Nijmegen"],"phenotypes":["Cardiomyopathy, dilated, 1LL"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":47,"hash_id":"55a4d99022c1fc6710839b84","name":"Dilated Cardiomyopathy and conduction defects","disease_group":"Cardiovascular disorders","disease_sub_group":"Cardiomyopathy","status":"public","version":"1.63","version_created":"2019-09-30T12:02:00.646768Z","relevant_disorders":["Dilated Cardiomyopathy","Dilated Cardiomyopathy (DCM)","Dilated cardiomyopathy - teen and adult"],"stats":{"number_of_genes":84,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["MEL1","PFM13","KIAA1675","MGC166915","KMT8F"],"biotype":"protein_coding","hgnc_id":"HGNC:14000","gene_name":"PR/SET domain 16","omim_gene":["605557"],"alias_name":["MDS1/EVI1-like","PR-domain zinc finger protein 16","transcription factor MEL1"],"gene_symbol":"PRDM16","hgnc_symbol":"PRDM16","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:2985732-3355185","ensembl_id":"ENSG00000142611"}},"GRch38":{"90":{"location":"1:3069168-3438621","ensembl_id":"ENSG00000142611"}}},"hgnc_date_symbol_changed":"2000-11-28"},"entity_type":"gene","entity_name":"PRDM16","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["London South GLH","Expert Review Red","London South GLH","Expert Review Red"],"phenotypes":["Left ventricular noncompaction 8","Cardiomyopathy, dilated, 1LL"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":750,"hash_id":null,"name":"Sudden cardiac death","disease_group":"","disease_sub_group":"","status":"public","version":"0.10","version_created":"2019-09-24T10:05:54.784946Z","relevant_disorders":["Molecular autopsy","R138"],"stats":{"number_of_genes":119,"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 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."}]}}]}