{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MPD"],"biotype":"protein_coding","hgnc_id":"HGNC:7529","gene_name":"mevalonate diphosphate decarboxylase","omim_gene":["603236"],"alias_name":["mevalonate pyrophosphate decarboxylase","diphosphomevalonate decarboxylase"],"gene_symbol":"MVD","hgnc_symbol":"MVD","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"16:88718343-88729569","ensembl_id":"ENSG00000167508"}},"GRch38":{"90":{"location":"16:88651935-88663161","ensembl_id":"ENSG00000167508"}}},"hgnc_date_symbol_changed":"1997-12-05"},"entity_type":"gene","entity_name":"MVD","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26202976","26816331 (correction for PMID:26202976)","28777842"],"evidence":["Expert Review Green","Other","Radboud University Medical Center, Nijmegen"],"phenotypes":["Porokeratosis 7, multiple types, 614714","actinic/non-actinic disseminated superficial porokeratosis","POROK7","DSAP/DSP"],"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"}]}}]}