Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7485
Gene Symbol: GET1
GET1
CUI: C0013080
Disease: Down Syndrome
Down Syndrome 		0.040 AlteredExpression BEFREE We concluded that the maternally inherited 5mCpG imprints at the WRB DMR are uncoupled from the parental allele expression of WRB and ten neighboring genes in several tissues and that trisomy 21 alters DNA methylation in parent-of-origin-dependent and -independent manners. 27100087

2016
Entrez Id: 7485
Gene Symbol: GET1
GET1
CUI: C0013080
Disease: Down Syndrome
Down Syndrome 		0.040 Biomarker BEFREE In humans, this CHD5/WRB is located between the markers ACTL5-D21S268 within the Down syndrome (DS) Region-2 at chromosome 21. 19207181

2009
Entrez Id: 7485
Gene Symbol: GET1
GET1
CUI: C0013080
Disease: Down Syndrome
Down Syndrome 		0.040 Biomarker BEFREE The understanding of the biological function of the protein product should clarify the potential role of WRB in the pathogenesis of DS CHD. 9544840

1998
Entrez Id: 7485
Gene Symbol: GET1
GET1
CUI: C0013080
Disease: Down Syndrome
Down Syndrome 		0.040 GeneticVariation BEFREE Additionally, we have accurately located a previously described gene, the WRB gene, between the markers ACTL5-D21S268 within this Down Syndrome Region-2. 9480850

1998