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Molecular autopsy

Gene: PSEN2

Amber List (moderate evidence)

PSEN2 (presenilin 2)
EnsemblGeneIds (GRCh38): ENSG00000143801
EnsemblGeneIds (GRCh37): ENSG00000143801
OMIM: 600759, Gene2Phenotype
PSEN2 is in 4 panels

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Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
Phenotypes
  • Cardiomyopathy, dilated, 1V
OMIM
600759
Clinvar variants
Variants in PSEN2
Penetrance
None
Panels with this gene

History Filter Activity

20 Dec 2018, Gel status: 2

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Ellen McDonagh (Genomics England Curator)

gene: PSEN2 was added gene: PSEN2 was added to Molecular autopsy. Sources: Expert Review Amber Mode of inheritance for gene: PSEN2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: PSEN2 were set to Cardiomyopathy, dilated, 1V