UBE3A Chromosome 15

Ubiquitin protein ligase E3A
249 variants 249 Health Risk

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What This Gene Does
This gene encodes an E3 ubiquitin-protein ligase, part of the ubiquitin protein degradation system. This imprinted gene is maternally expressed in brain and biallelically expressed in other tissues. Maternally inherited deletion of this gene causes Angelman Syndrome, characterized by severe motor and intellectual retardation, ataxia, hypotonia, epilepsy, absence of speech, and characteristic facies. The protein also interacts with the E6 protein of human papillomavirus types 16 and 18, resulting in ubiquitination and proteolysis of tumor protein p53. Alternative splicing of this gene results in three transcript variants encoding three isoforms with different N-termini. Additional transcript variants have been described, but their full length nature has not been determined. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
HECT domain containing
Locus Type
gene with protein product
Location
15q11.2
Ensembl
ENSG00000114062
Associated Conditions (9)
Intellectual disability
Angelman syndrome
Inborn genetic diseases
Developmental delay
See cases
UBE3A-related disorder
6 conditions
Epileptic encephalopathy
Neurodevelopmental disorder
Key Variants
All Variants (249)
RSID Category Clinical Significance Conditions
RS1312971608 Health Risk Conflicting classifications of pathogenicity Intellectual disability, Angelman syndrome, Intellectual disability
RS1398256620 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Angelman syndrome
RS1555393315 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Angelman syndrome
RS2152515457 Health Risk Conflicting classifications of pathogenicity
RS2552181678 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Angelman syndrome
RS369853017 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Angelman syndrome
RS376815580 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Inborn genetic diseases, Angelman syndrome
RS587782926 Health Risk Conflicting classifications of pathogenicity
RS587784517 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Angelman syndrome
RS587784523 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Angelman syndrome
RS587784524 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Inborn genetic diseases, Angelman syndrome
RS587784528 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Angelman syndrome
RS745363984 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Inborn genetic diseases, Angelman syndrome
RS746286431 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Angelman syndrome
RS755765955 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Angelman syndrome
RS780429591 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Angelman syndrome
RS943659663 Health Risk Conflicting classifications of pathogenicity Angelman syndrome, Inborn genetic diseases, Angelman syndrome
RS1057517876 Health Risk Likely pathogenic
RS1057518777 Health Risk Likely pathogenic Intellectual disability, Developmental delay, Intellectual disability
RS1057524508 Health Risk Likely pathogenic
RS1064795001 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS1064795012 Health Risk Likely pathogenic Angelman syndrome, Inborn genetic diseases, Angelman syndrome
RS111033597 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS1207660411 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS1445563777 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS1555380809 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS1555393242 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS1555399980 Health Risk Likely pathogenic
RS1566954813 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1566959617 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS1595362860 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS1595375255 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS1595376260 Health Risk Likely pathogenic
RS1595572384 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS1595591164 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS2074288628 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS2074492359 Health Risk Likely pathogenic Intellectual disability, Intellectual disability
RS2077166492 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS2077275624 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS2077884610 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS2152683847 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS2152693602 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS2152701181 Health Risk Likely pathogenic
RS2152819923 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS2152822637 Health Risk Likely pathogenic See cases, See cases
RS2152848080 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS2552181711 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS2552186527 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS2552186598 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
RS2552186646 Health Risk Likely pathogenic Angelman syndrome, Angelman syndrome
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