{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["GOLIM7"],"biotype":"protein_coding","hgnc_id":"HGNC:6824","gene_name":"mannosidase alpha class 2A member 1","omim_gene":["154582"],"alias_name":["golgi integral membrane protein 7"],"gene_symbol":"MAN2A1","hgnc_symbol":"MAN2A1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"5:109025067-109205326","ensembl_id":"ENSG00000112893"}},"GRch38":{"90":{"location":"5:109689366-109869625","ensembl_id":"ENSG00000112893"}}},"hgnc_date_symbol_changed":"1993-11-01"},"entity_type":"gene","entity_name":"MAN2A1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Expert list"],"phenotypes":["Homo sapiens mannosidase, alpha, class 2A, member 1 (MAN2A1), mRNA"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":230,"hash_id":"553f979fbb5a1616e5ed45f8","name":"Cataracts","disease_group":"Ophthalmological disorders","disease_sub_group":"Anterior segment abnormalities","status":"public","version":"2.0","version_created":"2019-10-02T14:52:22.701027Z","relevant_disorders":["R31"],"stats":{"number_of_genes":172,"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":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}