|
| 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 |
Combined analysis of keratinocyte cancers identifies novel genome-wide loci.
|
31174203 |
2019 |
|
| Entrez Id: |
7157 |
| Gene Symbol: |
TP53 |
TP53
|
0.130 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma.
|
27539887 |
2016 |
|
| Entrez Id: |
7157 |
| Gene Symbol: |
TP53 |
TP53
|
0.130 |
GeneticVariation
|
disease |
GWASCAT |
New basal cell carcinoma susceptibility loci.
|
25855136 |
2015 |
|
| Entrez Id: |
7157 |
| Gene Symbol: |
TP53 |
TP53
|
0.130 |
GeneticVariation
|
disease |
GWASCAT |
Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.
|
24403052 |
2014 |
|
| 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: |
7157 |
| Gene Symbol: |
TP53 |
TP53
|
0.130 |
AlteredExpression
|
disease |
LHGDN |
Phosphorylation state of tumor-suppressor gene p53 product overexpressed in skin tumors.
|
15492790 |
2004 |
|
| Entrez Id: |
7157 |
| Gene Symbol: |
TP53 |
TP53
|
0.130 |
GeneticVariation
|
disease |
LHGDN |
Mutations of the p53 and PTCH gene in basal cell carcinomas: UV mutation signature and strand bias.
|
12007715 |
2002 |
|
| Entrez Id: |
7157 |
| Gene Symbol: |
TP53 |
TP53
|
0.130 |
Biomarker
|
disease |
LHGDN |
Interaction between bcl-2 and P53 in neoplastic progression of basal cell carcinoma of the head and neck.
|
11911244 |
2002 |
|
| Entrez Id: |
4157 |
| Gene Symbol: |
MC1R |
MC1R
|
0.120 |
GeneticVariation
|
disease |
GWASCAT |
Combined analysis of keratinocyte cancers identifies novel genome-wide loci.
|
31174203 |
2019 |
|
| Entrez Id: |
4157 |
| Gene Symbol: |
MC1R |
MC1R
|
0.120 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma.
|
27539887 |
2016 |
|
| Entrez Id: |
4157 |
| Gene Symbol: |
MC1R |
MC1R
|
0.120 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma.
|
21700618 |
2011 |
|
| Entrez Id: |
4157 |
| Gene Symbol: |
MC1R |
MC1R
|
0.120 |
GeneticVariation
|
disease |
LHGDN |
MC1R variants associated susceptibility to basal cell carcinoma of skin: interaction with host factors and XRCC3 polymorphism.
|
18067130 |
2008 |
|
| Entrez Id: |
4157 |
| Gene Symbol: |
MC1R |
MC1R
|
0.120 |
GeneticVariation
|
disease |
LHGDN |
MC1R and PTCH gene polymorphism in French patients with basal cell carcinomas.
|
16645598 |
2006 |
|
| Entrez Id: |
7299 |
| Gene Symbol: |
TYR |
TYR
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Combined analysis of keratinocyte cancers identifies novel genome-wide loci.
|
31174203 |
2019 |
|
| Entrez Id: |
7299 |
| Gene Symbol: |
TYR |
TYR
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma.
|
27539887 |
2016 |
|
| 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: |
3662 |
| Gene Symbol: |
IRF4 |
IRF4
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Combined analysis of keratinocyte cancers identifies novel genome-wide loci.
|
31174203 |
2019 |