UBE3A:Ensemblv115

ubiquitin protein ligase E3A
OMIM: 601623, ClinGen, DECIPHER

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green UBE3A in Angelman Rett like syndromes


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green
Phenotypes
  • Angelman syndrome, MIM#105830
Tags
  • SV/CNV

Green UBE3A in Autism


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

0 reviews Unknown
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services

Green UBE3A in Cerebral Palsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Sources
  • Literature
  • Expert Review Green
Phenotypes
  • Angelman syndrome , OMIM #105830

Green UBE3A in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Sources
  • Victorian Clinical Genetics Services
  • Australian Genomics Health Alliance Epilepsy Flagship
  • Victorian Clinical Genetics Services
  • Expert Review Green
Phenotypes
  • Angelman syndrome, MIM#105830

Green UBE3A in Regression


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

0 reviews Unknown
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services

Green UBE3A in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Sources
  • Genetic Health Queensland
  • Expert Review Green
Phenotypes
  • Angelman syndrome MONDO:0007113

Green UBE3A in Imprinting disorders


Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Affected tissue: brain
  • Phenotype resulting from under expression: Angelman Syndrome