{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["DRE1","FLJ20059"],"biotype":"protein_coding","hgnc_id":"HGNC:25947","gene_name":"kelch like family member 24","omim_gene":["611295"],"alias_name":null,"gene_symbol":"KLHL24","hgnc_symbol":"KLHL24","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"3:183353356-183402265","ensembl_id":"ENSG00000114796"}},"GRch38":{"90":{"location":"3:183635568-183684477","ensembl_id":"ENSG00000114796"}}},"hgnc_date_symbol_changed":"2005-09-10"},"entity_type":"gene","entity_name":"KLHL24","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"Other - please provide details in the comments","publications":["Nat Genet. 2016 Dec","48(12):1508-1516. Am J Hum Genet. 2016 Dec 1","99(6):1395-1404. J Invest Dermatol. 2017 Jan 19. pii: S0022-202X(17)30032-5"],"evidence":["Expert Review Green","Literature"],"phenotypes":["Epidermolysis bullosa simplex (autosomal dominant)"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":119,"hash_id":"56310b9a22c1fc58285b282c","name":"Epidermolysis bullosa","disease_group":"Dermatological disorders","disease_sub_group":"Skin fragility disorders","status":"public","version":"1.6","version_created":"2019-01-07T16:40:38.182703Z","relevant_disorders":[],"stats":{"number_of_genes":21,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["DRE1","FLJ20059"],"biotype":"protein_coding","hgnc_id":"HGNC:25947","gene_name":"kelch like family member 24","omim_gene":["611295"],"alias_name":null,"gene_symbol":"KLHL24","hgnc_symbol":"KLHL24","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"3:183353356-183402265","ensembl_id":"ENSG00000114796"}},"GRch38":{"90":{"location":"3:183635568-183684477","ensembl_id":"ENSG00000114796"}}},"hgnc_date_symbol_changed":"2005-09-10"},"entity_type":"gene","entity_name":"KLHL24","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"Other - please provide details in the comments","publications":["99(6):1395-1404. J Invest Dermatol. 2017 Jan 19. pii: S0022-202X(17)30032-5","48(12):1508-1516. Am J Hum Genet. 2016 Dec 1","Nat Genet. 2016 Dec"],"evidence":["Expert Review Green"],"phenotypes":["Epidermolysis bullosa simplex (autosomal dominant)"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":554,"hash_id":null,"name":"Epidermolysis bullosa and congenital skin fragility","disease_group":"","disease_sub_group":"","status":"public","version":"0.16","version_created":"2019-09-17T18:43:54.606444Z","relevant_disorders":[],"stats":{"number_of_genes":46,"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"}]}}]}