{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["H2-KE4","D6S2244E","KE4","RING5","ZIP7"],"biotype":"protein_coding","hgnc_id":"HGNC:4927","gene_name":"solute carrier family 39 member 7","omim_gene":["601416"],"alias_name":null,"gene_symbol":"SLC39A7","hgnc_symbol":"SLC39A7","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:33168222-33172216","ensembl_id":"ENSG00000112473"}},"GRch38":{"90":{"location":"6:33200445-33204439","ensembl_id":"ENSG00000112473"}}},"hgnc_date_symbol_changed":"2003-10-27"},"entity_type":"gene","entity_name":"SLC39A7","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":554,"hash_id":null,"name":"Epidermolysis bullosa and congenital skin fragility","disease_group":"","disease_sub_group":"","status":"public","version":"0.16","version_created":"2019-09-17T18:43:54.606444Z","relevant_disorders":[],"stats":{"number_of_genes":46,"number_of_strs":0,"number_of_regions":0},"types":[{"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)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}