Beckwith-Wiedemann Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A syndrome characterized by overgrowth (macrosomia), an increased risk of childhood cancer and congenital malformations. (Human Disease Ontology, DOID_5572)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D001506
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Genes

5 genes/proteins associated with the disease Beckwith-Wiedemann Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
IGF2 insulin-like growth factor 2 2.88009
KCNQ1OT1 KCNQ1 opposite strand/antisense transcript 1 (non-protein coding) 2.88009
H19 H19, imprinted maternally expressed transcript (non-protein coding) 2.88009
NSD1 nuclear receptor binding SET domain protein 1 2.88009
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2) 2.88009