Gene: WDR19 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57728
Gene Symbol: WDR19
WDR19 		0.610 CausalMutation disease CLINVAR Next-generation sequencing-based molecular diagnosis of 35 Hispanic retinitis pigmentosa probands. 27596865 2016
Entrez Id: 57728
Gene Symbol: WDR19
WDR19 		0.610 CausalMutation disease CLINVAR Nephronophthisis 13: implications of its association with Caroli disease and altered intracellular localization of WDR19 in the kidney. 25726036 2015
Entrez Id: 57728
Gene Symbol: WDR19
WDR19 		0.610 AlteredExpression disease BEFREE In this study, we visually validated the expression pattern of mutant WDR19 protein in the kidneys of NPHP 13 patients. 25726036 2015
Entrez Id: 57728
Gene Symbol: WDR19
WDR19 		0.610 Biomarker disease GENOMICS_ENGLAND Mutations in WDR19 encoding the intraflagellar transport component IFT144 cause a broad spectrum of ciliopathies. 24504730 2014
Entrez Id: 57728
Gene Symbol: WDR19
WDR19 		0.610 CausalMutation disease CLINVAR WDR19: an ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior-Loken syndrome. 23683095 2013
Entrez Id: 57728
Gene Symbol: WDR19
WDR19 		0.610 CausalMutation disease CLINVAR Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathy. 23559409 2013
Entrez Id: 57728
Gene Symbol: WDR19
WDR19 		0.610 GeneticVariation disease UNIPROT Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19. 22019273 2011
Entrez Id: 57728
Gene Symbol: WDR19
WDR19 		0.610 Biomarker disease GENOMICS_ENGLAND