Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3670
Gene Symbol: ISL1
ISL1
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.030 GeneticVariation BEFREE As a result, a new heterozygous ISL1 mutation, NM_002202.2: c.225C>G; p. (Tyr75*), was discovered in an index patient with double outlet right ventricle and ventricular septal defect. 31484864

2019
Entrez Id: 3670
Gene Symbol: ISL1
ISL1
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.030 Biomarker BEFREE ISL1 is related to the atrial septal defect group and the ventricular septal defect group, and the genotypes were associated with the occurrence of CHD in the dominant mode of inheritance. 24634231

2014
Entrez Id: 3670
Gene Symbol: ISL1
ISL1
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.030 GeneticVariation BEFREE These findings suggest that ISL1 genetic polymorphisms are associated with occurrence of VSD, thus they may be useful as molecular markers for prediction of VSD. 23572340

2013