Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80312
Gene Symbol: TET1
TET1
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		0.020 Biomarker BEFREE Our study reveals a mechanism how L1 elements get activated in the absence of Mecp2 and suggests that Tet1 may contribute to Mecp2/Mbd2-deficiency phenotypes, such as the Rett syndrome. 28524723

2017
Entrez Id: 80312
Gene Symbol: TET1
TET1
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		0.020 Biomarker BEFREE Accordingly, we find 5-hydroxymethylcytosine enriched at heterochromatin of Mecp2-deficient neurons of a mouse model for Rett syndrome and Tet1-induced reexpression of silenced major satellite repeats. 27923996

2017