Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55130
Gene Symbol: ARMC4
ARMC4
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry. 23849778

2013

Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker 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
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, 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: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD A complex syndrome of left-right axis, central nervous system and axial skeleton defects in Zic3 mutant mice. 11959836

2002

Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, 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: 7547
Gene Symbol: ZIC3
ZIC3
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, 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: 93
Gene Symbol: ACVR2B
ACVR2B
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD The signaling pathway mediated by the type IIB activin receptor controls axial patterning and lateral asymmetry in the mouse. 9242489

1997

Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD The interfrontal bone and mutant genes in the mouse. 1018005

1976

Entrez Id: 7547
Gene Symbol: ZIC3
ZIC3
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD """Bent-Tail,"" A Dominant, Sex-Linked Mutation in the Mouse." 16589192

1952

Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 339804
Gene Symbol: C2orf74
C2orf74
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 284403
Gene Symbol: WDR62
WDR62
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 118856
Gene Symbol: MMP21
MMP21
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 91147
Gene Symbol: TMEM67
TMEM67
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 5125
Gene Symbol: PCSK5
PCSK5
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 1954
Gene Symbol: MEGF8
MEGF8
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 80173
Gene Symbol: IFT74
IFT74
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 80184
Gene Symbol: CEP290
CEP290
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 55997
Gene Symbol: CFC1
CFC1
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 79363
Gene Symbol: CPLANE2
CPLANE2
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 8928
Gene Symbol: FOXH1
FOXH1
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 1767
Gene Symbol: DNAH5
DNAH5
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD

Entrez Id: 9353
Gene Symbol: SLIT2
SLIT2
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
0.200 Biomarker MGD