Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 GeneticVariation BEFREE Angelman syndrome (AS) is a rare neurodevelopmental disorder caused by mutation or deletion of the maternally inherited UBE3A allele. 31490639

2020

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 GeneticVariation BEFREE Angelman syndrome (AS) is a congenital neuro-developmental disorder typically occurring due to functional defects of the UBE3A gene caused by uniparental disomy (UPD), translocation or single gene mutation. 31173236

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 AlteredExpression BEFREE Delayed loss of UBE3A reduces the expression of Angelman syndrome-associated phenotypes. 31143434

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 GeneticVariation BEFREE As compared to training with massed trials, spaced training significantly improved learning in both the Ts65Dn trisomy mouse model of Down syndrome and the maternally inherited Ube3a mutant mouse model of Angelman syndrome. 31182707

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 AlteredExpression BEFREE Loss of E6AP expression leads to the development of Angelman syndrome (AS), clinically characterized by lack of speech, abnormal motor development, and the presence of seizures. 31114479

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 AlteredExpression BEFREE This study tested the hypothesis that by increasing the methylation of the UBE3A-antisense transcript in Angelman syndrome to promote expression of the silenced paternal UBE3A gene we may ameliorate the clinical phenotypes of AS. 31640736

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 GeneticVariation BEFREE Our results provide strong evidence for the contribution of non-UBE3A neuronal pathophysiology in deletion AS and suggest that hemizygosity of the GABRB3-GABRA5-GABRG3 gene cluster causes abnormal theta and beta EEG oscillations that may underlie the more severe clinical phenotype. 30826071

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 Biomarker BEFREE Thus, our results identify HAP1 as an in vivo UBE3A target that contributes to deregulated autophagy and synaptic dysfunction in the central nervous system of AS mouse. 31445164

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 AlteredExpression BEFREE The observed differences in sex-dependent neurobehavioral phenotypes and the differential transcriptome expression profiles in AS mice strengthen the evidence for molecular cross talk between Ube3a protein and sex hormone receptors or their elicited pathways. 30706369

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 Biomarker BEFREE Taken together, our findings elucidate the mechanisms underlying the subcellular localization of UBE3A, and indicate that the nuclear UBE3A isoform is the most critical for the pathophysiology of Angelman syndrome. 31235931

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 Biomarker BEFREE Since its discovery, the E3 ubiquitin ligase E6-associated protein (E6AP) has been studied extensively in two pathological contexts: infection by the human papillomavirus (HPV), and the neurodevelopmental disorder, Angelman syndrome. 31087000

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 AlteredExpression BEFREE We found that loss of axonal contact guidance is specific for AS neurons while UBE3A overexpression does not affect neuronal directional polarization along microgratings. 31798818

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 GeneticVariation BEFREE The primary genetic cause of Angelman syndrome is a maternally transmitted mutation in the Ube3a gene, which has been successfully modeled in Ube3a mutant mice. 31730795

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 GeneticVariation BEFREE We established human induced pluripotent stem cells (iPSCs) from an Angelman syndrome patient with the deletion of maternal 15q11.2-q13 including UBE3A gene. 30605843

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 Biomarker BEFREE Removal of this element led to up-regulation of <i>UBE3A-ATS</i> without repressing paternal <i>UBE3A</i> However, increasing expression of <i>UBE3A-ATS</i> in the absence of the boundary element resulted in full repression of paternal <i>UBE3A</i>, demonstrating that <i>UBE3A</i> imprinting requires both the loss of function from the boundary element as well as the up-regulation of <i>UBE3A-ATS</i> These results suggest that manipulation of the competition between <i>UBE3A-ATS</i> and <i>UBE3A</i> may provide a potential therapeutic approach for AS. 30674673

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 AlteredExpression BEFREE Angelman syndrome (AS) is a neurogenetic disorder associated with impaired expression of the ubiquitin-protein ligase E3A gene on chromosome 15. 30681431

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 Biomarker BEFREE Deficiency in the E3 ubiquitin ligase UBE3A leads to the neurodevelopmental disorder Angelman syndrome (AS), while additional dosage of UBE3A is linked to autism spectrum disorder. 31160454

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 Biomarker BEFREE Here, we implemented the flurothyl kindling and retest paradigm in AS model mice to assess epileptogenesis and to gain mechanistic insights owed to loss of maternal Ube3a. 30352049

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 GeneticVariation BEFREE Previous studies of UBE3A function have not examined full Ube3a deletion in mouse, the complexity of imprinted gene networks in brain, nor the molecular basis of systems-level cognitive dysfunctions in Angelman syndrome. 31625566

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 AlteredExpression BEFREE The complete characterization of the ubiquitination pathway of an UBE3A substrate is important due to the role of this E3 ligase in rare neurological disorders as Angelman syndrome. 31130875

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 Biomarker BEFREE Genome-wide transcriptome analysis revealed an enrichment of genes downstream of interferon regulatory factor (IRF) in a UBE3A-deficient AS mouse model. 30690483

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 GeneticVariation BEFREE Angelman syndrome (AS) is a neurodevelopmental disorder caused by the loss of function of the maternal copy of the UBE3A gene. 31401139

2019

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 GeneticVariation BEFREE Exome sequencing revealed a previously unreported mutation of Ubiquitin Protein Ligase E3A (UBE3A) gene, confirming the diagnosis of Angelman syndrome. 29250725

2018

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 GeneticVariation BEFREE Perturbations in activity and dosage of the UBE3A ubiquitin-ligase have been linked to Angelman syndrome and autism spectrum disorders. 29426014

2018

Entrez Id: 7337
Gene Symbol: UBE3A
UBE3A
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
1.000 Biomarker BEFREE These anatomical data may help to elucidate the role of UBE3A in Angelman syndrome and autism spectrum disorder. 30364390

2018