×
Entrez Id:
1437
Gene Symbol:
CSF2
CSF2
0.300
Therapeutic
disease
CTD_human
Valproic acid-induced fetal malformations are reduced by maternal immune stimulation with granulocyte-macrophage colony-stimulating factor or interferon-gamma.
17075842
2006
×
Entrez Id:
2350
Gene Symbol:
FOLR2
FOLR2
0.300
Biomarker
disease
CTD_human
Arsenic-induced congenital malformations in genetically susceptible folate binding protein-2 knockout mice.
11749123
2001
×
Entrez Id:
3458
Gene Symbol:
IFNG
IFNG
0.300
Therapeutic
disease
CTD_human
Valproic acid-induced fetal malformations are reduced by maternal immune stimulation with granulocyte-macrophage colony-stimulating factor or interferon-gamma.
17075842
2006
×
Entrez Id:
85416
Gene Symbol:
ZIC5
ZIC5
0.300
Biomarker
disease
CTD_human
Mouse Zic5 deficiency results in neural tube defects and hypoplasia of cephalic neural crest derivatives.
15136147
2004
×
Entrez Id:
5077
Gene Symbol:
PAX3
PAX3
0.300
Biomarker
disease
CTD_human
Histological comparison of the effects of the splotch gene and retinoic acid on the closure of the mouse neural tube.
3293260
1988
×
Entrez Id:
6347
Gene Symbol:
CCL2
CCL2
0.300
Biomarker
disease
CTD_human
×
Entrez Id:
1544
Gene Symbol:
CYP1A2
CYP1A2
0.300
Biomarker
disease
CTD_human
Caffeine, selected metabolic gene variants, and risk for neural tube defects.
20641098
2010
×
Entrez Id:
4522
Gene Symbol:
MTHFD1
MTHFD1
0.300
Biomarker
disease
CTD_human
A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: report of the Birth Defects Research Group.
12384833
2002
×
Entrez Id:
80199
Gene Symbol:
FUZ
FUZ
0.300
Biomarker
disease
CTD_human
×
Entrez Id:
5652
Gene Symbol:
PRSS8
PRSS8
0.300
Therapeutic
disease
CTD_human
Functional analysis of a missense mutation in the serine protease inhibitor SPINT2 associated with congenital sodium diarrhea.
24722141
2014
×
Entrez Id:
57822
Gene Symbol:
GRHL3
GRHL3
0.300
Biomarker
disease
CTD_human
Differential response of heterozygous curly-tail mouse embryos to vitamin A teratogenesis depending on maternal genotype.
6635991
1983
×
Entrez Id:
5697
Gene Symbol:
PYY
PYY
0.300
Biomarker
disease
CTD_human
Gastrointestinal hormones (anorexigenic peptide YY and orexigenic ghrelin) influence neural tube development.
17400914
2007
×
Entrez Id:
635
Gene Symbol:
BHMT
BHMT
0.300
Biomarker
disease
CTD_human
Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions.
17035141
2006
×
Entrez Id:
51738
Gene Symbol:
GHRL
GHRL
0.300
Therapeutic
disease
CTD_human
Gastrointestinal hormones (anorexigenic peptide YY and orexigenic ghrelin) influence neural tube development.
17400914
2007
×
Entrez Id:
5077
Gene Symbol:
PAX3
PAX3
0.300
Therapeutic
disease
CTD_human
Histological comparison of the effects of the splotch gene and retinoic acid on the closure of the mouse neural tube.
3293260
1988
×
Entrez Id:
7546
Gene Symbol:
ZIC2
ZIC2
0.300
Biomarker
disease
CTD_human
Mouse Zic5 deficiency results in neural tube defects and hypoplasia of cephalic neural crest derivatives.
15136147
2004
×
Entrez Id:
10653
Gene Symbol:
SPINT2
SPINT2
0.300
Biomarker
disease
CTD_human
Functional analysis of a missense mutation in the serine protease inhibitor SPINT2 associated with congenital sodium diarrhea.
24722141
2014
×
Entrez Id:
6862
Gene Symbol:
TBXT
TBXT
0.300
Biomarker
disease
CTD_human
×
Entrez Id:
27443
Gene Symbol:
CECR2
CECR2
0.300
Biomarker
disease
CTD_human
CECR2, a protein involved in neurulation, forms a novel chromatin remodeling complex with SNF2L.
15640247
2005
×
Entrez Id:
4524
Gene Symbol:
MTHFR
MTHFR
0.300
Biomarker
disease
CTD_human
Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studies.
23056169
2012
×
Entrez Id:
5077
Gene Symbol:
PAX3
PAX3
0.300
Therapeutic
disease
CTD_human
Oxidant regulation of gene expression and neural tube development: Insights gained from diabetic pregnancy on molecular causes of neural tube defects.
12739027
2003
×
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:
5077
Gene Symbol:
PAX3
PAX3
0.300
Therapeutic
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:
10
Gene Symbol:
NAT2
NAT2
0.300
Biomarker
disease
CTD_human
Caffeine, selected metabolic gene variants, and risk for neural tube defects.
20641098
2010
×
Entrez Id:
6240
Gene Symbol:
RRM1
RRM1
0.300
Biomarker
disease
CTD_human
Ribonucleotide reductase subunit R1: a gene conferring sensitivity to valproic acid-induced neural tube defects in mice.
10716750
2000