Gene: CCN1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3491
Gene Symbol: CCN1
CCN1 		0.210 GeneticVariation group BEFREE Our study is the first to suggest a relationship between a probable CCN1 mutation and ASD. 25135600 2015
Entrez Id: 3491
Gene Symbol: CCN1
CCN1 		0.210 Biomarker group MGD Together, these results provide evidence that deficiency in matrix signaling can lead to autosomal dominant AVSD, identify Ccn1(+/-) mice as a genetic model for ostium primum ASD, and implicate CCN1 as a candidate gene for AVSD in humans. 17023674 2006