{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA1010","Tuba","ARHGEF36"],"biotype":"protein_coding","hgnc_id":"HGNC:30373","gene_name":"dynamin binding protein","omim_gene":["611282"],"alias_name":["scaffold protein TUBA"],"gene_symbol":"DNMBP","hgnc_symbol":"DNMBP","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"10:101635334-101769676","ensembl_id":"ENSG00000107554"}},"GRch38":{"90":{"location":"10:99875577-100009919","ensembl_id":"ENSG00000107554"}}},"hgnc_date_symbol_changed":"2004-04-05"},"entity_type":"gene","entity_name":"DNMBP","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["30290152"],"evidence":["Expert list","Expert Review Green"],"phenotypes":["Cataract 48, 618415"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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."}]}}]}