{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PIGPC1","dJ496H19.1","KCP1","THW","KRTCAP1"],"biotype":"protein_coding","hgnc_id":"HGNC:17637","gene_name":"PERP, TP53 apoptosis effector","omim_gene":["609301"],"alias_name":["keratinocyte associated protein 1"],"gene_symbol":"PERP","hgnc_symbol":"PERP","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:138409642-138428648","ensembl_id":"ENSG00000112378"}},"GRch38":{"90":{"location":"6:138088505-138107511","ensembl_id":"ENSG00000112378"}}},"hgnc_date_symbol_changed":"2003-11-19"},"entity_type":"gene","entity_name":"PERP","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["30321533"],"evidence":["London North GLH","NHS GMS","Expert Review Red"],"phenotypes":["Dominant and Recessive Keratoderma"],"mode_of_inheritance":"BOTH monoallelic and biallelic, autosomal or pseudoautosomal","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"}]}}]}