Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 81839
Gene Symbol: VANGL1
VANGL1 		0.600 GeneticVariation disease UNIPROT Novel mutations in VANGL1 in neural tube defects. 19319979 2009
Entrez Id: 81839
Gene Symbol: VANGL1
VANGL1 		0.600 Biomarker disease GENOMICS_ENGLAND Mutations in VANGL1 associated with neural-tube defects. 17409324 2007
Entrez Id: 81839
Gene Symbol: VANGL1
VANGL1 		0.600 GeneticVariation disease UNIPROT Mutations in VANGL1 associated with neural-tube defects. 17409324 2007
Entrez Id: 81839
Gene Symbol: VANGL1
VANGL1 		0.600 SusceptibilityMutation disease CLINVAR
Entrez Id: 6862
Gene Symbol: TBXT
TBXT 		0.400 GeneticVariation disease UNIPROT Autozygome and high throughput confirmation of disease genes candidacy. 30237576 2019
Entrez Id: 56288
Gene Symbol: PARD3
PARD3 		0.400 CausalMutation disease CLINVAR Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation. 27925688 2017
Entrez Id: 56288
Gene Symbol: PARD3
PARD3 		0.400 SusceptibilityMutation disease CLINVAR Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation. 27925688 2017
Entrez Id: 56288
Gene Symbol: PARD3
PARD3 		0.400 GeneticVariation disease UNIPROT Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation. 27925688 2017
Entrez Id: 9620
Gene Symbol: CELSR1
CELSR1 		0.400 GeneticVariation disease UNIPROT Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis. 22095531 2012
Entrez Id: 57216
Gene Symbol: VANGL2
VANGL2 		0.400 GeneticVariation disease UNIPROT VANGL2 mutations in human cranial neural-tube defects. 20558380 2010
Entrez Id: 6862
Gene Symbol: TBXT
TBXT 		0.400 GeneticVariation disease UNIPROT The human T locus and spina bifida risk. 15449172 2004
Entrez Id: 57216
Gene Symbol: VANGL2
VANGL2 		0.400 SusceptibilityMutation disease CLINVAR
Entrez Id: 9620
Gene Symbol: CELSR1
CELSR1 		0.400 SusceptibilityMutation disease CLINVAR
Entrez Id: 80199
Gene Symbol: FUZ
FUZ 		0.400 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 80199
Gene Symbol: FUZ
FUZ 		0.400 SusceptibilityMutation disease CLINVAR
Entrez Id: 6862
Gene Symbol: TBXT
TBXT 		0.400 SusceptibilityMutation disease CLINVAR
Entrez Id: 23513
Gene Symbol: SCRIB
SCRIB 		0.300 GeneticVariation disease UNIPROT Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis. 22095531 2012
Entrez Id: 51339
Gene Symbol: DACT1
DACT1 		0.300 GeneticVariation disease UNIPROT Identification of novel rare mutations of DACT1 in human neural tube defects. 22610794 2012
Entrez Id: 4524
Gene Symbol: MTHFR
MTHFR 		0.100 SusceptibilityMutation disease CLINVAR
Entrez Id: 10395
Gene Symbol: DLC1
DLC1 		0.100 SusceptibilityMutation disease CLINVAR
Entrez Id: 3688
Gene Symbol: ITGB1
ITGB1 		0.100 SusceptibilityMutation disease CLINVAR