{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:3631","gene_name":"farnesyl diphosphate synthase","omim_gene":["134629"],"alias_name":["farnesyl pyrophosphate synthetase, dimethylallyltranstransferase, geranyltranstransferase"],"gene_symbol":"FDPS","hgnc_symbol":"FDPS","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:155278539-155290457","ensembl_id":"ENSG00000160752"}},"GRch38":{"90":{"location":"1:155308748-155320666","ensembl_id":"ENSG00000160752"}}},"hgnc_date_symbol_changed":"1992-03-13"},"entity_type":"gene","entity_name":"FDPS","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26202976","26816331 (correction for PMID:26202976)","27422687"],"evidence":["Expert Review Green","Radboud University Medical Center, Nijmegen","Other"],"phenotypes":["Porokeratosis 9, multiple types, 616631","DSAP/DSP","actinic or nonactinic disseminated superficial porokeratosis","POROK9"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":["deletions"],"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"}]}}]}