{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["Hb-1"],"biotype":"protein_coding","hgnc_id":"HGNC:6458","gene_name":"keratin 81","omim_gene":["602153"],"alias_name":["hard keratin type II 1"],"gene_symbol":"KRT81","hgnc_symbol":"KRT81","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"12:52679697-52685318","ensembl_id":"ENSG00000205426"}},"GRch38":{"90":{"location":"12:52285913-52291534","ensembl_id":"ENSG00000205426"}}},"hgnc_date_symbol_changed":"2006-07-17"},"entity_type":"gene","entity_name":"KRT81","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber"],"phenotypes":[],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":553,"hash_id":null,"name":"Ectodermal dysplasia","disease_group":"","disease_sub_group":"","status":"public","version":"0.22","version_created":"2019-09-17T19:00:33.930109Z","relevant_disorders":[],"stats":{"number_of_genes":71,"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"}]}}]}