{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["TMTSP"],"biotype":"protein_coding","hgnc_id":"HGNC:17754","gene_name":"thrombospondin type 1 domain containing 1","omim_gene":["616821"],"alias_name":null,"gene_symbol":"THSD1","hgnc_symbol":"THSD1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"13:52951305-52980629","ensembl_id":"ENSG00000136114"}},"GRch38":{"90":{"location":"13:52377167-52406494","ensembl_id":"ENSG00000136114"}}},"hgnc_date_symbol_changed":"2003-01-24"},"entity_type":"gene","entity_name":"THSD1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["27895300"],"evidence":["Expert Review Green","Literature"],"phenotypes":["subarachnoid hemorrhage"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":147,"hash_id":"5819a24f8f6203341de99c89","name":"Cerebral vascular malformations","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Cerebrovascular disorders","status":"public","version":"1.47","version_created":"2019-09-13T13:47:21.970257Z","relevant_disorders":["Cerebrovascular disorders","Vein of Galen malformation","Cerebral arteriovenous malformations","Moyamoya disease"],"stats":{"number_of_genes":95,"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."}]}}]}