{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["B3GNT-2","BETA3GNT","B3GN-T2","B3GN-T1"],"biotype":"protein_coding","hgnc_id":"HGNC:15629","gene_name":"UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2","omim_gene":["605581"],"alias_name":null,"gene_symbol":"B3GNT2","hgnc_symbol":"B3GNT2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"2:62423248-62451866","ensembl_id":"ENSG00000170340"}},"GRch38":{"90":{"location":"2:62196113-62224731","ensembl_id":"ENSG00000170340"}}},"hgnc_date_symbol_changed":"2006-04-12"},"entity_type":"gene","entity_name":"B3GNT2","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["23359570","23877401"],"evidence":["NHS GMS","Expert Review Amber","Other"],"phenotypes":["Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13  615287"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":["watchlist"],"panel":{"id":179,"hash_id":"5763f35c8f620350a22bccdf","name":"Hydrocephalus","disease_group":"","disease_sub_group":"","status":"public","version":"1.38","version_created":"2019-09-30T12:37:55.307389Z","relevant_disorders":["Hydrocephalus;R86"],"stats":{"number_of_genes":98,"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 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"}]}}]}