Gene: WT1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7490
Gene Symbol: WT1
WT1 		0.510 Biomarker phenotype CTD_human Genetic factors in congenital diaphragmatic hernia. 17436238 2007
Entrez Id: 7490
Gene Symbol: WT1
WT1 		0.510 Biomarker phenotype MGD Teratogen-induced, dietary and genetic models of congenital diaphragmatic hernia share a common mechanism of pathogenesis. 17071579 2006
Entrez Id: 7490
Gene Symbol: WT1
WT1 		0.510 Biomarker phenotype MGD The Wilms tumor suppressor gene wt1 is required for development of the spleen. 10469569 1999
Entrez Id: 7490
Gene Symbol: WT1
WT1 		0.510 AlteredExpression phenotype BEFREE The expression of the WT1 gene in pleural and abdominal mesothelium and the occurrence of diaphragmatic hernia in transgenic mice with a homozygous WT1 deletion strongly suggests that the diaphragmatic hernia in this patient is part of the malformation pattern caused by WT1 mutations. 7645607 1995