Mosaic Variegated Aneuploidy Syndrome Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	Mosaic variegated aneuploidy (MVA) syndrome is a chromosomal anomaly characterized by multiple mosaic aneuploidies that leads to a variety of phenotypic abnormalities and cancer predisposition. (Orphanet Rare Disease Ontology, Orphanet_1052)
External Link	https://www.disgenet.org/browser/0/1/0/C1850343
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Genes

9 genes associated with the disease Mosaic Variegated Aneuploidy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
APC	adenomatous polyposis coli
BUB1	BUB1 mitotic checkpoint serine/threonine kinase
BUB1B	BUB1 mitotic checkpoint serine/threonine kinase B
BUB3	BUB3 mitotic checkpoint protein
CD19	CD19 molecule
CEP57	centrosomal protein 57kDa
CNTN3	contactin 3 (plasmacytoma associated)
PAK6	p21 protein (Cdc42/Rac)-activated kinase 6
TRIP13	thyroid hormone receptor interactor 13