{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["HBVES","POP1","POPDC1"],"biotype":"protein_coding","hgnc_id":"HGNC:1152","gene_name":"blood vessel epicardial substance","omim_gene":["604577"],"alias_name":["popeye domain containing 1"],"gene_symbol":"BVES","hgnc_symbol":"BVES","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:105544697-105585049","ensembl_id":"ENSG00000112276"}},"GRch38":{"90":{"location":"6:105096822-105137174","ensembl_id":"ENSG00000112276"}}},"hgnc_date_symbol_changed":"2000-01-10"},"entity_type":"gene","entity_name":"BVES","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["26642364"],"evidence":["Expert Review Red"],"phenotypes":["Muscular dystrophy, limb-girdle, type 2X"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":465,"hash_id":null,"name":"Neuromuscular disorders","disease_group":"","disease_sub_group":"","status":"public","version":"1.11","version_created":"2019-10-09T12:42:27.875560Z","relevant_disorders":["Other rare neuromuscular disorders; R381"],"stats":{"number_of_genes":245,"number_of_strs":2,"number_of_regions":5},"types":[{"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"}]}},{"gene_data":{"alias":["HBVES","POP1","POPDC1"],"biotype":"protein_coding","hgnc_id":"HGNC:1152","gene_name":"blood vessel epicardial substance","omim_gene":["604577"],"alias_name":["popeye domain containing 1"],"gene_symbol":"BVES","hgnc_symbol":"BVES","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"6:105544697-105585049","ensembl_id":"ENSG00000112276"}},"GRch38":{"90":{"location":"6:105096822-105137174","ensembl_id":"ENSG00000112276"}}},"hgnc_date_symbol_changed":"2000-01-10"},"entity_type":"gene","entity_name":"BVES","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26642364"],"evidence":["Yorkshire and North East GLH","NHS GMS","South West GLH","Expert Review Red","Literature"],"phenotypes":["Muscular dystrophy, limb-girdle, type 2X, 616812","limb girdle muscular dystrophy","cardiac arrhythmia"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":185,"hash_id":"55b7a65322c1fc05fc7a1869","name":"Limb girdle muscular dystrophy","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neuromuscular disorders","status":"public","version":"1.89","version_created":"2019-06-20T15:15:12.994579Z","relevant_disorders":[],"stats":{"number_of_genes":84,"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","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"}]}}]}