{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MICE","MGC119078","MGC119079"],"biotype":"protein_coding","hgnc_id":"HGNC:1502","gene_name":"caspase 14","omim_gene":["605848"],"alias_name":["apoptosis-related cysteine protease"],"gene_symbol":"CASP14","hgnc_symbol":"CASP14","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:15160195-15169104","ensembl_id":"ENSG00000105141"}},"GRch38":{"90":{"location":"19:15049384-15058293","ensembl_id":"ENSG00000105141"}}},"hgnc_date_symbol_changed":"1998-11-09"},"entity_type":"gene","entity_name":"CASP14","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["London North GLH","NHS GMS","Expert Review Green"],"phenotypes":["Ichthyosis, congenital, autosomal recessive 12","617320"],"mode_of_inheritance":"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"}]}}]}