squamous cell carcinoma Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A carcinoma that derives_from squamous epithelial cells. (Human Disease Ontology, DOID_1749)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002860
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17 genes associated with the squamous cell carcinoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BLM Bloom syndrome, RecQ helicase-like
CDKN2A cyclin-dependent kinase inhibitor 2A
COL7A1 collagen, type VII, alpha 1
DDB2 damage-specific DNA binding protein 2, 48kDa
DKC1 dyskeratosis congenita 1, dyskerin
ERCC3 excision repair cross-complementation group 3
GJB2 gap junction protein, beta 2, 26kDa
ING1 inhibitor of growth family, member 1
POLH polymerase (DNA directed), eta
PTEN phosphatase and tensin homolog
RECQL4 RecQ protein-like 4
SLX4 SLX4 structure-specific endonuclease subunit
TERC telomerase RNA component
TNFRSF10B tumor necrosis factor receptor superfamily, member 10b
WNT10A wingless-type MMTV integration site family, member 10A
WRAP53 WD repeat containing, antisense to TP53
XPC xeroderma pigmentosum, complementation group C