Port-Wine Stain Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A congenital vascular malformation consisting of superficial and deep dilated capillaries in the skin which produce a reddish to purplish discolouration of the skin. (Human Phenotype Ontology, HP_0001052)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D019339
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Genes

2 genes/proteins associated with the disease Port-Wine Stain from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
RASA1 RAS p21 protein activator (GTPase activating protein) 1 2.88009
GNAQ guanine nucleotide binding protein (G protein), q polypeptide 2.88009