Gene: VANGL2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57216
Gene Symbol: VANGL2
VANGL2 		0.330 Biomarker disease BEFREE Vangl2 disruption alters the biomechanics of late spinal neurulation leading to spina bifida in mouse embryos. 29590636 2018
Entrez Id: 57216
Gene Symbol: VANGL2
VANGL2 		0.330 GeneticVariation disease BEFREE Overexpression of Grainyhead-like 3 causes spina bifida and interacts genetically with mutant alleles of Grhl2 and Vangl2 in mice. 30189017 2018
Entrez Id: 57216
Gene Symbol: VANGL2
VANGL2 		0.330 Biomarker disease BEFREE Protein tyrosine kinase 7 (Ptk7) was shown to cause a very severe form of NTDs called craniorachischisis in a mouse model and genetically interacts with a core PCP member Vangl2 where double heterozygotes suffer from spina bifida. 26368655 2015
Entrez Id: 57216
Gene Symbol: VANGL2
VANGL2 		0.330 Biomarker disease CTD_human A novel hypomorphic Looptail allele at the planar cell polarity Vangl2 gene. 21404367 2011