{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["TER","MRT14"],"biotype":"protein_coding","hgnc_id":"HGNC:4551","gene_name":"trans-2,3-enoyl-CoA reductase","omim_gene":["610057"],"alias_name":null,"gene_symbol":"TECR","hgnc_symbol":"TECR","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"19:14627897-14676792","ensembl_id":"ENSG00000099797"}},"GRch38":{"90":{"location":"19:14517085-14565980","ensembl_id":"ENSG00000099797"}}},"hgnc_date_symbol_changed":"2009-07-21"},"entity_type":"gene","entity_name":"TECR","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["21212097"],"evidence":["Victorian Clinical Genetics Services","Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["non-syndromic mental retardation"],"mode_of_inheritance":"","tags":["founder-effect"],"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"}]}}]}