Gene: WDR73 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 84942
Gene Symbol: WDR73
WDR73 		0.400 Biomarker disease GENOMICS_ENGLAND Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73. 26070982 2015
Entrez Id: 84942
Gene Symbol: WDR73
WDR73 		0.400 GeneticVariation disease CLINVAR Loss-of-function mutations in WDR73 are responsible for microcephaly and steroid-resistant nephrotic syndrome: Galloway-Mowat syndrome. 25466283 2014
Entrez Id: 84942
Gene Symbol: WDR73
WDR73 		0.400 Biomarker disease GENOMICS_ENGLAND Loss-of-function mutations in WDR73 are responsible for microcephaly and steroid-resistant nephrotic syndrome: Galloway-Mowat syndrome. 25466283 2014
Entrez Id: 84942
Gene Symbol: WDR73
WDR73 		0.400 Biomarker disease GENOMICS_ENGLAND Perinatal imaging findings of Galloway-Mowat syndrome. 18019379 2007
Entrez Id: 84942
Gene Symbol: WDR73
WDR73 		0.400 CausalMutation disease CLINVAR
Entrez Id: 84942
Gene Symbol: WDR73
WDR73 		0.400 Biomarker disease GENOMICS_ENGLAND