{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ23412","VNUT"],"biotype":"protein_coding","hgnc_id":"HGNC:16192","gene_name":"solute carrier family 17 member 9","omim_gene":["612107"],"alias_name":null,"gene_symbol":"SLC17A9","hgnc_symbol":"SLC17A9","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"20:61584052-61599949","ensembl_id":"ENSG00000101194"}},"GRch38":{"90":{"location":"20:62952647-62969585","ensembl_id":"ENSG00000101194"}}},"hgnc_date_symbol_changed":"2009-01-22"},"entity_type":"gene","entity_name":"SLC17A9","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["25180256","25596766 (article in French)"],"evidence":["Expert Review Amber","Other","Radboud University Medical Center, Nijmegen"],"phenotypes":["Porokeratosis 8, disseminated superficial actinic type, 616063","disseminated superficial actinic porokeratosis-8","POROK8","Disseminated superficial actinic porokeratosis (DSAP)"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":["watchlist"],"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"}]}}]}