Xeroderma pigmentosum Gene Set

Dataset PhosphoSitePlus Phosphosite-Disease Associations
Category disease or phenotype associations
Type disease
Description An autosomal recessive disease that is characterized by a deficiency in the ability to repair ultraviolet damage that has_material_basis_in autosomal recessive inheritance of DNA repair. (Human Disease Ontology, DOID_0050427)
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Genes

1 proteins associated with the disease Xeroderma pigmentosum from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Symbol Name
RARA retinoic acid receptor, alpha