Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5 		0.200 Biomarker disease MGD Point mutations in murine Nkx2-5 phenocopy human congenital heart disease and induce pathogenic Wnt signaling. 28352650 2017
Entrez Id: 2626
Gene Symbol: GATA4
GATA4 		0.200 Biomarker disease MGD Congenital heart disease-causing Gata4 mutation displays functional deficits in vivo. 22589735 2012
Entrez Id: 4908
Gene Symbol: NTF3
NTF3 		0.200 Biomarker disease MGD LIG family receptor tyrosine kinase-associated proteins modulate growth factor signals during neural development. 19755105 2009
Entrez Id: 3491
Gene Symbol: CCN1
CCN1 		0.200 Biomarker disease MGD The matricellular protein CCN1 is essential for cardiac development. 17023674 2006
Entrez Id: 4908
Gene Symbol: NTF3
NTF3 		0.200 Biomarker disease MGD Loss of brain-derived neurotrophic factor-dependent neural crest-derived sensory neurons in neurotrophin-4 mutant mice. 10681461 2000
Entrez Id: 4908
Gene Symbol: NTF3
NTF3 		0.200 Biomarker disease MGD Absence of sensory neurons before target innervation in brain-derived neurotrophic factor-, neurotrophin 3-, and TrkC-deficient embryonic mice. 9364058 1997
Entrez Id: 4908
Gene Symbol: NTF3
NTF3 		0.200 Biomarker disease MGD Identification of an essential nonneuronal function of neurotrophin 3 in mammalian cardiac development. 8841198 1996
Entrez Id: 4908
Gene Symbol: NTF3
NTF3 		0.200 Biomarker disease MGD Targeted mutation in the neurotrophin-3 gene results in loss of muscle sensory neurons. 7991545 1994
Entrez Id: 414
Gene Symbol: ARSD
ARSD 		0.010 Biomarker disease BEFREE Coronary Sinus Defect Following Transcatheter Closure of ASD Using Amplatzer Septal Occluder: Potential Erosion by the Device. 28396933 2017