{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["VRP"],"biotype":"protein_coding","hgnc_id":"HGNC:12682","gene_name":"vascular endothelial growth factor C","omim_gene":["601528"],"alias_name":["vascular endothelial growth factor-related protein"],"gene_symbol":"VEGFC","hgnc_symbol":"VEGFC","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"4:177604689-177713881","ensembl_id":"ENSG00000150630"}},"GRch38":{"90":{"location":"4:176683538-176792727","ensembl_id":"ENSG00000150630"}}},"hgnc_date_symbol_changed":"1996-10-26"},"entity_type":"gene","entity_name":"VEGFC","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["23410910","24744435","14634646","30071673"],"evidence":["London South GLH","Expert Review Green","Expert list"],"phenotypes":["Lymphedema, hereditary, ID\t615907 (Primary Lymphoedema, Milroy-like)"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":65,"hash_id":"57ee82ef8f62035c9b2d0487","name":"Primary lymphoedema","disease_group":"Cardiovascular disorders","disease_sub_group":"Lymphatic Disorders","status":"public","version":"2.0","version_created":"2019-10-02T14:10:33.689992Z","relevant_disorders":["Lymphatic Disorders","Meiges disease","Meige disease","Milroy disease","Lymphoedema distichiasis","Lipoedema disease","R136"],"stats":{"number_of_genes":51,"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."}]}}]}