Source: MGD

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 339804
Gene Symbol: C2orf74
C2orf74
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		0.200 Biomarker MGD

Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		0.200 Biomarker 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
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		0.200 Biomarker MGD The interfrontal bone and mutant genes in the mouse. 1018005

1976
Entrez Id: 5125
Gene Symbol: PCSK5
PCSK5
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		0.200 Biomarker MGD

Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		0.200 Biomarker 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
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		0.200 Biomarker MGD A deletion encompassing Zic3 in bent tail, a mouse model for X-linked neural tube defects. 10861288

2000
Entrez Id: 1767
Gene Symbol: DNAH5
DNAH5
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		0.200 Biomarker MGD

Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		0.200 Biomarker MGD

Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		0.200 Biomarker MGD Zic3 is required in the migrating primitive streak for node morphogenesis and left-right patterning. 23303524

2013
Entrez Id: 55130
Gene Symbol: ARMC4
ARMC4
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		0.200 Biomarker MGD ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry. 23849778

2013