{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["bTrCP","betaTrCP","FBXW1A","Fwd1","beta-TrCP1","bTrCP1"],"biotype":"protein_coding","hgnc_id":"HGNC:1144","gene_name":"beta-transducin repeat containing E3 ubiquitin protein ligase","omim_gene":["603482"],"alias_name":null,"gene_symbol":"BTRC","hgnc_symbol":"BTRC","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"10:103113820-103317078","ensembl_id":"ENSG00000166167"}},"GRch38":{"90":{"location":"10:101354033-101557321","ensembl_id":"ENSG00000166167"}}},"hgnc_date_symbol_changed":"1999-01-28"},"entity_type":"gene","entity_name":"BTRC","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"Other - please provide details in the comments","publications":["12913067","29263051","28777841","28422522","27600068","23596994","16691619"],"evidence":["Expert Review Amber","London South East RGC GSTT","Viapath"],"phenotypes":["Split-hand split-foot malformation 3"],"mode_of_inheritance":"","tags":["cnv","microduplication"],"panel":{"id":384,"hash_id":null,"name":"Limb disorders","disease_group":"","disease_sub_group":"","status":"public","version":"1.61","version_created":"2019-10-03T10:01:34.398179Z","relevant_disorders":[],"stats":{"number_of_genes":234,"number_of_strs":0,"number_of_regions":1},"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"}]}}]}