{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["GPSN2L","SRD5A2L2","DKFZp313D0829","DKFZp313B2333","TERL"],"biotype":"protein_coding","hgnc_id":"HGNC:27365","gene_name":"trans-2,3-enoyl-CoA reductase like","omim_gene":["617242"],"alias_name":["glycoprotein, synaptic 2-like"],"gene_symbol":"TECRL","hgnc_symbol":"TECRL","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:65140975-65275186","ensembl_id":"ENSG00000205678"}},"GRch38":{"90":{"location":"4:64275257-64409468","ensembl_id":"ENSG00000205678"}}},"hgnc_date_symbol_changed":"2009-07-21"},"entity_type":"gene","entity_name":"TECRL","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["27861123"],"evidence":["Expert Review Amber","South West GLH"],"phenotypes":["Ventricular tachycardia, catecholaminergic polymorphic, 3 614021"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":214,"hash_id":"55a3aac122c1fc6710839b7d","name":"Catecholaminergic polymorphic VT","disease_group":"Cardiovascular disorders","disease_sub_group":"Cardiac arrhythmia","status":"public","version":"1.25","version_created":"2019-10-02T11:14:32.240274Z","relevant_disorders":["Catecholaminergic Polymorphic Ventricular Tachycardia","R129"],"stats":{"number_of_genes":10,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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)"}]}}]}