Gene: UBE3B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 89910
Gene Symbol: UBE3B
UBE3B 		0.110 GeneticVariation disease BEFREE We conclude that UBE3B mutations cause a clinically recognizable and possibly underdiagnosed syndrome characterized by distinct craniofacial features, hypotonia, failure to thrive, eye abnormalities, other congenital malformations, low cholesterol levels, and severe intellectual disability. 24615390 2014
Entrez Id: 89910
Gene Symbol: UBE3B
UBE3B 		0.110 Biomarker disease HPO