{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["DLNB11"],"biotype":"protein_coding","hgnc_id":"HGNC:23688","gene_name":"B-cell CLL/lymphoma 9 like","omim_gene":["609004"],"alias_name":null,"gene_symbol":"BCL9L","hgnc_symbol":"BCL9L","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"11:118764584-118796317","ensembl_id":"ENSG00000186174"}},"GRch38":{"90":{"location":"11:118893875-118925608","ensembl_id":"ENSG00000186174"}}},"hgnc_date_symbol_changed":"2003-12-09"},"entity_type":"gene","entity_name":"BCL9L","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["23035047"],"evidence":["Expert Review Amber","Literature"],"phenotypes":["Heterotaxy"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":478,"hash_id":null,"name":"Fetal anomalies","disease_group":"","disease_sub_group":"","status":"public","version":"0.344","version_created":"2019-09-17T09:38:10.568007Z","relevant_disorders":["R21"],"stats":{"number_of_genes":1721,"number_of_strs":0,"number_of_regions":0},"types":[{"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."}]}}]}