{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CDHF1"],"biotype":"protein_coding","hgnc_id":"HGNC:3035","gene_name":"desmocollin 1","omim_gene":["125643"],"alias_name":null,"gene_symbol":"DSC1","hgnc_symbol":"DSC1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"18:28709199-28742819","ensembl_id":"ENSG00000134765"}},"GRch38":{"90":{"location":"18:31129236-31162856","ensembl_id":"ENSG00000134765"}}},"hgnc_date_symbol_changed":"1991-09-25"},"entity_type":"gene","entity_name":"DSC1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["London North GLH","NHS GMS","Expert Review Red"],"phenotypes":["Desmosomal disorders"],"mode_of_inheritance":"","tags":[],"panel":{"id":556,"hash_id":null,"name":"Palmoplantar keratodermas","disease_group":"","disease_sub_group":"","status":"public","version":"0.9","version_created":"2019-09-09T15:38:38.871976Z","relevant_disorders":[],"stats":{"number_of_genes":69,"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"}]}}]}