Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR 		0.300 Biomarker disease CTD_human Genetic variation associated with the occurrence and progression of neurological disorders. 27713094 2017
Entrez Id: 57216
Gene Symbol: VANGL2
VANGL2 		0.300 Biomarker disease CTD_human A novel hypomorphic Looptail allele at the planar cell polarity Vangl2 gene. 21404367 2011
Entrez Id: 5444
Gene Symbol: PON1
PON1 		0.300 Biomarker disease CTD_human Paraoxonase 1 polymorphisms and haplotypes and the risk for having offspring affected with spina bifida in Southeast Mexico. 21031563 2010
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		0.300 Biomarker disease CTD_human Genetic polymorphisms in the thioredoxin 2 (TXN2) gene and risk for spina bifida. 19165900 2009
Entrez Id: 5077
Gene Symbol: PAX3
PAX3 		0.300 Biomarker disease CTD_human Screening for novel PAX3 polymorphisms and risks of spina bifida. 17149730 2007
Entrez Id: 1072
Gene Symbol: CFL1
CFL1 		0.300 Biomarker disease CTD_human Association between CFL1 gene polymorphisms and spina bifida risk in a California population. 17352815 2007
Entrez Id: 5130
Gene Symbol: PCYT1A
PCYT1A 		0.300 Biomarker disease CTD_human CHKA and PCYT1A gene polymorphisms, choline intake and spina bifida risk in a California population. 17184542 2006
Entrez Id: 1119
Gene Symbol: CHKA
CHKA 		0.300 Biomarker disease CTD_human CHKA and PCYT1A gene polymorphisms, choline intake and spina bifida risk in a California population. 17184542 2006
Entrez Id: 5110
Gene Symbol: PCMT1
PCMT1 		0.300 Biomarker disease CTD_human A known functional polymorphism (Ile120Val) of the human PCMT1 gene and risk of spina bifida. 16256389 2006
Entrez Id: 6347
Gene Symbol: CCL2
CCL2 		0.300 Biomarker disease CTD_human Maternal genotype for the monocyte chemoattractant protein 1 A(-2518)G promoter polymorphism is associated with the risk of spina bifida in offspring. 16596675 2006
Entrez Id: 5077
Gene Symbol: PAX3
PAX3 		0.300 Biomarker disease CTD_human Effect of arsenite, maternal age, and embryonic sex on spina bifida, exencephaly, and resorption rates in the splotch mouse. 12854658 2003
Entrez Id: 5156
Gene Symbol: PDGFRA
PDGFRA 		0.300 Biomarker disease CTD_human A human YAC transgene rescues craniofacial and neural tube development in PDGFRalpha knockout mice and uncovers a role for PDGFRalpha in prenatal lung growth. 11023856 2000
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2 		0.300 Biomarker disease CTD_human FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndrome. 9605588 1998
Entrez Id: 5077
Gene Symbol: PAX3
PAX3 		0.300 Biomarker disease CTD_human Experimental teratological studies with the mouse CNS mutations cranioschisis and delayed splotch. 3902948 1985
Entrez Id: 5077
Gene Symbol: PAX3
PAX3 		0.300 Biomarker disease CTD_human Gene-teratogen interaction and its morphological basis in retinoic acid-induced mouse spina bifida. 6385329 1984