{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["JCL-1","BCG1","11B6","MAGE-D2","HCA10","MAGED","MGC8386"],"biotype":"protein_coding","hgnc_id":"HGNC:16353","gene_name":"MAGE family member D2","omim_gene":["300470"],"alias_name":["hepatocellular carcinoma associated protein","breast cancer associated gene 1","melanoma-associated antigen D2","hepatocellular carcinoma-associated protein HCA10"],"gene_symbol":"MAGED2","hgnc_symbol":"MAGED2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"X:54834032-54842445","ensembl_id":"ENSG00000102316"}},"GRch38":{"90":{"location":"X:54807599-54816012","ensembl_id":"ENSG00000102316"}}},"hgnc_date_symbol_changed":"2001-08-16"},"entity_type":"gene","entity_name":"MAGED2","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["27120771"],"evidence":["Expert Review Green","NHS GMS"],"phenotypes":["Bartter syndrome, type 5, antenatal, transient, 300971"],"mode_of_inheritance":"X-LINKED: hemizygous mutation in males, biallelic mutations in females","tags":[],"panel":{"id":292,"hash_id":"553f94d5bb5a1616e5ed45a4","name":"Renal tubulopathies","disease_group":"Renal and urinary tract disorders","disease_sub_group":"Disorders of function","status":"public","version":"1.193","version_created":"2019-10-09T09:34:39.432250Z","relevant_disorders":["Renal tubular acidosis","R198"],"stats":{"number_of_genes":55,"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)"}]}}]}