Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3 		0.910 Biomarker disease BEFREE The phenotype of these mice correctly models the defects found in human HTX1 and indicates an important role for Zic3 in both left-right and axial patterning. 11959836 2002
Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3 		0.910 GeneticVariation disease CLINVAR
Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3 		0.910 CausalMutation disease CLINVAR
Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3 		0.910 Biomarker disease CTD_human
Entrez Id: 55534
Gene Symbol: MAML3
MAML3 		0.100 GeneticVariation disease GWASCAT A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations. 23708190 2013
Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3 		0.910 Biomarker disease MGD The interfrontal bone and mutant genes in the mouse. 1018005 1976
Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3 		0.910 Biomarker disease MGD A deletion encompassing Zic3 in bent tail, a mouse model for X-linked neural tube defects. 10861288 2000
Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3 		0.910 Biomarker disease MGD Zic3 is required in the migrating primitive streak for node morphogenesis and left-right patterning. 23303524 2013
Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3 		0.910 Biomarker disease MGD The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus. 10942421 2000
Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3 		0.910 Biomarker disease MGD Zic3 is required in the extra-cardiac perinodal region of the lateral plate mesoderm for left-right patterning and heart development. 23184148 2013
Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3 		0.910 Biomarker disease MGD The phenotype of these mice correctly models the defects found in human HTX1 and indicates an important role for Zic3 in both left-right and axial patterning. 11959836 2002
Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3 		0.910 Biomarker disease MGD """Bent-Tail,"" A Dominant, Sex-Linked Mutation in the Mouse." 16589192 1952
Entrez Id: 79363
Gene Symbol: CPLANE2
CPLANE2 		0.200 Biomarker disease MGD
Entrez Id: 92749
Gene Symbol: DRC1
DRC1 		0.200 Biomarker disease MGD
Entrez Id: 5991
Gene Symbol: RFX3
RFX3 		0.200 Biomarker disease MGD
Entrez Id: 284403
Gene Symbol: WDR62
WDR62 		0.200 Biomarker disease MGD
Entrez Id: 9353
Gene Symbol: SLIT2
SLIT2 		0.200 Biomarker disease MGD
Entrez Id: 1767
Gene Symbol: DNAH5
DNAH5 		0.200 Biomarker disease MGD
Entrez Id: 57545
Gene Symbol: CC2D2A
CC2D2A 		0.200 Biomarker disease MGD
Entrez Id: 162
Gene Symbol: AP1B1
AP1B1 		0.200 Biomarker disease MGD
Entrez Id: 339804
Gene Symbol: C2orf74
C2orf74 		0.200 Biomarker disease MGD
Entrez Id: 8928
Gene Symbol: FOXH1
FOXH1 		0.200 Biomarker disease MGD
Entrez Id: 352909
Gene Symbol: DNAAF3
DNAAF3 		0.200 Biomarker disease MGD
Entrez Id: 55130
Gene Symbol: ARMC4
ARMC4 		0.200 Biomarker disease MGD ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry. 23849778 2013
Entrez Id: 221322
Gene Symbol: TBC1D32
TBC1D32 		0.200 Biomarker disease MGD