{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["PMK","PMKA","HUMPMKI"],"biotype":"protein_coding","hgnc_id":"HGNC:9141","gene_name":"phosphomevalonate kinase","omim_gene":["607622"],"alias_name":null,"gene_symbol":"PMVK","hgnc_symbol":"PMVK","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:154897210-154909467","ensembl_id":"ENSG00000163344"}},"GRch38":{"90":{"location":"1:154924734-154936991","ensembl_id":"ENSG00000163344"}}},"hgnc_date_symbol_changed":"1999-07-09"},"entity_type":"gene","entity_name":"PMVK","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26202976","26816331 (correction for PMID:26202976)","27052676"],"evidence":["Expert Review Red","Other"],"phenotypes":["Porokeratosis 1, multiple types, 175800","POROKERATOSIS OF MIBELLI"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":110,"hash_id":"5763f6048f620350a1996052","name":"Familial disseminated superficial actinic porokeratosis","disease_group":"Dermatological disorders","disease_sub_group":"Keratodermas","status":"public","version":"1.1","version_created":"2017-11-05T02:37:20.048842Z","relevant_disorders":[],"stats":{"number_of_genes":7,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}