basal cell carcinoma Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A skin carcinoma affecting basal cells. (Human Disease Ontology, DOID_2513)
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19 genes associated with the basal cell carcinoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CYLD cylindromatosis (turban tumor syndrome)
DDB2 damage-specific DNA binding protein 2, 48kDa
ERCC3 excision repair cross-complementation group 3
HRAS Harvey rat sarcoma viral oncogene homolog
KRAS Kirsten rat sarcoma viral oncogene homolog
MLH1 mutL homolog 1
MSH2 mutS homolog 2
MSH6 mutS homolog 6
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
POLH polymerase (DNA directed), eta
PTCH1 patched 1
PTCH2 patched 2
RASA1 RAS p21 protein activator (GTPase activating protein) 1
RECQL4 RecQ protein-like 4
SUFU suppressor of fused homolog (Drosophila)
TMC6 transmembrane channel-like 6
TMC8 transmembrane channel-like 8
WNT10A wingless-type MMTV integration site family, member 10A
XPC xeroderma pigmentosum, complementation group C