{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["HSBLMHC1","BTL-II","BTN7"],"biotype":"protein_coding","hgnc_id":"HGNC:1142","gene_name":"butyrophilin like 2","omim_gene":["606000"],"alias_name":null,"gene_symbol":"BTNL2","hgnc_symbol":"BTNL2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:32361740-32374905","ensembl_id":"ENSG00000204290"}},"GRch38":{"90":{"location":"6:32393963-32407128","ensembl_id":"ENSG00000204290"}}},"hgnc_date_symbol_changed":"2000-08-22"},"entity_type":"gene","entity_name":"BTNL2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":105,"hash_id":"572c908e8f62036eed0a39c8","name":"Pneumothorax - familial","disease_group":"Respiratory disorders","disease_sub_group":"Structural lung disorders","status":"public","version":"1.18","version_created":"2019-09-27T18:57:12.249816Z","relevant_disorders":["Familial Pneumothorax","Familial Primary Spontaneous Pneumothorax","R190"],"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)"}]}}]}