{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CHR10SYT"],"biotype":"protein_coding","hgnc_id":"HGNC:17167","gene_name":"synaptotagmin 15","omim_gene":["608081"],"alias_name":null,"gene_symbol":"SYT15","hgnc_symbol":"SYT15","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"10:46955444-46971400","ensembl_id":"ENSG00000204176"}},"GRch38":{"90":{"location":"10:46578217-46594173","ensembl_id":"ENSG00000204176"}}},"hgnc_date_symbol_changed":"2003-06-05"},"entity_type":"gene","entity_name":"SYT15","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","Wessex and West Midlands GLH"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":232,"hash_id":"553f94c2bb5a1616e5ed459c","name":"Congenital myaesthenic syndrome","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neuromuscular disorders","status":"public","version":"1.52","version_created":"2019-08-07T14:24:09.650638Z","relevant_disorders":["Congenital myaesthenia","Congenital myasthenia"],"stats":{"number_of_genes":35,"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)"}]}}]}