Source: MGD

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
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: 203286
Gene Symbol: ANKS6
ANKS6
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		0.200 Biomarker MGD

Entrez Id: 162
Gene Symbol: AP1B1
AP1B1
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		0.200 Biomarker MGD

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: 80114
Gene Symbol: BICC1
BICC1
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		0.200 Biomarker MGD

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: 57545
Gene Symbol: CC2D2A
CC2D2A
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: 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: 653275
Gene Symbol: CFC1B
CFC1B
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: 352909
Gene Symbol: DNAAF3
DNAAF3
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: 1767
Gene Symbol: DNAH5
DNAH5
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		0.200 Biomarker MGD

Entrez Id: 27019
Gene Symbol: DNAI1
DNAI1
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		0.200 Biomarker MGD

Entrez Id: 92749
Gene Symbol: DRC1
DRC1
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: 80173
Gene Symbol: IFT74
IFT74
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: 118856
Gene Symbol: MMP21
MMP21
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: 5991
Gene Symbol: RFX3
RFX3
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