{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["DUTT1","FLJ21882","SAX3"],"biotype":"protein_coding","hgnc_id":"HGNC:10249","gene_name":"roundabout guidance receptor 1","omim_gene":["602430"],"alias_name":null,"gene_symbol":"ROBO1","hgnc_symbol":"ROBO1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:78646390-79816965","ensembl_id":"ENSG00000169855"}},"GRch38":{"90":{"location":"3:78597240-79767815","ensembl_id":"ENSG00000169855"}}},"hgnc_date_symbol_changed":"1998-03-26"},"entity_type":"gene","entity_name":"ROBO1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["28592524","28485101","30712880"],"evidence":["Expert Review Green","PAGE Additional Gene List"],"phenotypes":["tetralogy of Fallot and septal defects"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","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."}]}}]}