×
Entrez Id:
7050
Gene Symbol:
TGIF1
TGIF1
0.010
GeneticVariation
disease
BEFREE
The study focused on the associated brain malformations, including neuronal migration defects, which predominated in individuals with ZIC2 mutations, and neural tube defects, which were frequently associated with ZIC2 (rachischisis ) and TGIF mutations.
21940735
2011
×
Entrez Id:
7546
Gene Symbol:
ZIC2
ZIC2
0.010
GeneticVariation
disease
BEFREE
The study focused on the associated brain malformations, including neuronal migration defects, which predominated in individuals with ZIC2 mutations, and neural tube defects, which were frequently associated with ZIC2 (rachischisis ) and TGIF mutations.
21940735
2011
×
Entrez Id:
3586
Gene Symbol:
IL10
IL10
0.010
GeneticVariation
disease
BEFREE
The study focused on the associated brain malformations, including neuronal migration defects, which predominated in individuals with ZIC2 mutations, and neural tube defects, which were frequently associated with ZIC2 (rachischisis ) and TGIF mutations.
21940735
2011
×
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:
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:
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:
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:
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:
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:
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:
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