Ichthyosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of the skin characterized the presence of excessive amounts of dry surface scales on the skin resulting from an abnormality of keratinization. (Human Phenotype Ontology, HP_0008064)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D007057
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Genes

3 genes/proteins associated with the disease Ichthyosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SUPV3L1 suppressor of var1, 3-like 1 (S. cerevisiae) 2.88009
GJB2 gap junction protein, beta 2, 26kDa 2.88009
PNPLA1 patatin-like phospholipase domain containing 1 2.88009