poikiloderma Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Poikiloderma refers to a patch of skin with (1) reticulated hypopigmentation and hyperpigmentation, (2) wrinkling secondary to epidermal atrophy, and (3) telangiectasias. (Human Phenotype Ontology, HP_0001029)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001029
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Genes

10 genes associated with the poikiloderma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DDB2 damage-specific DNA binding protein 2, 48kDa
ERCC2 excision repair cross-complementation group 2
ERCC6 excision repair cross-complementation group 6
FAM111B family with sequence similarity 111, member B
FERMT1 fermitin family member 1
POLH polymerase (DNA directed), eta
RECQL4 RecQ protein-like 4
USB1 U6 snRNA biogenesis 1
XPA xeroderma pigmentosum, complementation group A
XPC xeroderma pigmentosum, complementation group C