Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		0.030 Biomarker BEFREE Quantitative real-time RT-PCR analysis of PWS and AS samples with paternal and maternal 15q11-13 deletions revealed a paternal expression bias of GABRB3, while RTT brain samples showed a significant reduction in GABRB3 and UBE3A. 17339270

2007
Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		0.030 AlteredExpression BEFREE Here, we tested the hypothesis that MeCP2 deficiency affects expression of Ube3a in mouse models of RTT. 16754645

2006
Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		0.030 AlteredExpression BEFREE MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression. 15757975

2005