Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5727
Gene Symbol: PTCH1
PTCH1 		0.600 CausalMutation disease CGI
Entrez Id: 6608
Gene Symbol: SMO
SMO 		0.320 CausalMutation disease CGI
Entrez Id: 7507
Gene Symbol: XPA
XPA 		0.320 CausalMutation disease CGI
Entrez Id: 2068
Gene Symbol: ERCC2
ERCC2 		0.310 CausalMutation disease CGI
Entrez Id: 1643
Gene Symbol: DDB2
DDB2 		0.300 CausalMutation disease CGI
Entrez Id: 2071
Gene Symbol: ERCC3
ERCC3 		0.300 CausalMutation disease CGI
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B 		0.300 CausalMutation disease CGI
Entrez Id: 2072
Gene Symbol: ERCC4
ERCC4 		0.300 CausalMutation disease CGI
Entrez Id: 2073
Gene Symbol: ERCC5
ERCC5 		0.300 CausalMutation disease CGI
Entrez Id: 5921
Gene Symbol: RASA1
RASA1 		0.300 CausalMutation disease CGI
Entrez Id: 7508
Gene Symbol: XPC
XPC 		0.300 CausalMutation disease CGI
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.130 GeneticVariation disease GWASCAT A germline variant in the TP53 polyadenylation signal confers cancer susceptibility. 21946351 2011
Entrez Id: 5727
Gene Symbol: PTCH1
PTCH1 		0.600 GeneticVariation disease LHGDN A new mutation of PTCH gene in a Chinese family with nevoid basal cell carcinoma syndrome. 18272036 2008
Entrez Id: 5727
Gene Symbol: PTCH1
PTCH1 		0.600 GeneticVariation disease LHGDN A novel germ-line mutation of PTCH1 gene in a Japanese family of nevoid basal cell carcinoma syndrome: are the palmoplantar pits associated with true basal cell carcinoma? 18436435 2008
Entrez Id: 5727
Gene Symbol: PTCH1
PTCH1 		0.600 GeneticVariation disease LHGDN A novel PTCH1 mutation in a patient of nevoid basal cell carcinoma syndrome. 18068337 2008
Entrez Id: 3685
Gene Symbol: ITGAV
ITGAV 		0.010 Biomarker disease LHGDN alpha vbeta 6 Integrin promotes the invasion of morphoeic basal cell carcinoma through stromal modulation. 18451156 2008
Entrez Id: 3621
Gene Symbol: ING1
ING1 		0.010 AlteredExpression disease LHGDN Analyses of the tumour suppressor ING1 expression and gene mutation in human basal cell carcinoma. 12632089 2003
Entrez Id: 7299
Gene Symbol: TYR
TYR 		0.110 GeneticVariation disease LHGDN ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma. 18488027 2008
Entrez Id: 434
Gene Symbol: ASIP
ASIP 		0.010 GeneticVariation disease LHGDN ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma. 18488027 2008
Entrez Id: 841
Gene Symbol: CASP8
CASP8 		0.100 GeneticVariation disease GWASCAT Association between genetic variation within vitamin D receptor-DNA binding sites and risk of basal cell carcinoma. 28177523 2017
Entrez Id: 22891
Gene Symbol: ZNF365
ZNF365 		0.100 GeneticVariation disease GWASCAT Association between genetic variation within vitamin D receptor-DNA binding sites and risk of basal cell carcinoma. 28177523 2017
Entrez Id: 5743
Gene Symbol: PTGS2
PTGS2 		0.020 GeneticVariation disease LHGDN Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. 17578436 2007
Entrez Id: 7124
Gene Symbol: TNF
TNF 		0.010 GeneticVariation disease LHGDN Basal cell carcinoma is associated with high TNF-alpha release but nor with TNF-alpha polymorphism at position--308. 14714556 2003
Entrez Id: 26585
Gene Symbol: GREM1
GREM1 		0.010 AlteredExpression disease LHGDN Bone morphogenetic protein antagonist gremlin 1 is widely expressed by cancer-associated stromal cells and can promote tumor cell proliferation. 17003113 2006
Entrez Id: 652
Gene Symbol: BMP4
BMP4 		0.010 AlteredExpression disease LHGDN Bone morphogenetic protein antagonist gremlin 1 is widely expressed by cancer-associated stromal cells and can promote tumor cell proliferation. 17003113 2006