Upregulated genes |
ABCB1
|
+3.63 |
7q21.12 |
Decreases drug accumulation |
ABCC1
|
+1.25 |
16p13.11 |
Involves in multi-drug resistance |
ABCC2
|
+1.00 |
10q24.2 |
Involves in multi-drug resistance |
ABCC3
|
+1.02 |
17q21.33 |
Involves in multi-drug resistance |
ABCC5
|
+1.01 |
3q27.1 |
Provides resistance to thiopurine anticancer drugs |
ABCG2
|
+1.69 |
4q22.1 |
Responses to mitoxantrone and anthracycline exposure |
ACTB
|
+1.16 |
7p22.1 |
Involves in cell motility, structure, integrity, and intercellular signaling |
AHR
|
+1.45 |
7p21.1 |
Regulate xenobiotic-metabolizing enzymes |
AR
|
+2.03 |
Xq12 |
Encode polyglutamine and polyglycine tracts |
ATM
|
+1.01 |
11q22.3 |
Cell response to DNA damage |
B2M
|
+1.14 |
15q21.1 |
Association with the MHC |
BCL2L1
|
+1.14 |
20q11.21 |
Apoptotic inhibitor |
BLMH
|
+1.02 |
17q11.2 |
Metabolic inactivation |
BRCA1
|
+1.13 |
17q21.31 |
Maintains genomic stability |
BRCA2
|
+1.62 |
13q13.1 |
Involves in maintenance of genome stability |
CCND1
|
+1.12 |
11q13.3 |
Required for cell cycle G1/S transition |
CCNE1
|
+1.13 |
19q12 |
Required for cell cycle G1/S transition |
CDK2
|
+1.29 |
12q13.2 |
Regulates progression through the cell cycle |
CDK4
|
+1.02 |
12q14.1 |
Regulates progression through the cell cycle |
CLPTM1L
|
+1.67 |
5p15.33 |
Increases susceptibility to cancers |
CYP2C19
|
+2.24 |
10q23.33 |
Variable ability to metabolize mephenytoin |
CYP2C8
|
+1.53 |
10q23.33 |
Anticonvulsive drug mephenytoin |
CYP2E1
|
+2.02 |
10q26.3 |
Involves in drug metabolism |
CYP3A5
|
+1.46 |
18q21.1 |
Involves in drug metabolism |
DHFR
|
+1.00 |
5q14.1 |
Identified on separate chromosomes |
EGFR
|
+1.10 |
7p11.2 |
Promotes cell proliferation |
ELK1
|
+1.25 |
Xp11.23 |
Promotes cell proliferation |
ESR1
|
+1.07 |
6q25.1-q25.2 |
A ligand-activated transcription |
ESR2
|
+1.49 |
14q23.2-q23.3 |
Inhibits cell proliferation |
FGF2
|
+1.27 |
4q28.1 |
Nervous system development, wound healing, and tumor growth |
FOS
|
+1.26 |
14q24.3 |
Cell proliferation and transformation |
GSTP1
|
+1.02 |
11q13.2 |
Reduces glutathione and detoxification |
HPRT1
|
+1.05 |
Xq26.2-q26.3 |
Plays a central role in the generation of purine nucleotides |
MET
|
+1.40 |
7q31.2 |
Induces dimerization and activation of the receptor, |
MSH2
|
+1.18 |
2p21-p16.3 |
Consistent with the characteristic alterations |
MYC
|
+1.31 |
8q24.21 |
Participates in cell cycle progression, apoptosis and cellular transformation |
NAT2
|
+1.19 |
8p22. |
Associated with higher incidences of cancer and drug toxicity |
NFKB2
|
+1.03 |
10q24.32 |
Involves in inflammation and immune function |
PPARA
|
+1.27 |
22q13.31 |
Promotes proliferation |
PPARG
|
+1.74 |
3p25.2 |
A regulator of adipocyte differentiation |
RARB
|
+1.64 |
3p24.2 |
Mediates signaling in cell growth and differentiation |
SULT1E1
|
+2.11 |
4q13.3 |
Controls levels of estrogen receptors |
TNFRSF11A
|
+1.00 |
18q21.33 |
Promotes proliferation |
UGCG
|
+1.41 |
9q31.3 |
The core structure of many glycosphingolipids |
Downregulated genes |
XPA
|
−1.00 |
9q22.33 |
Plays a central role in nucleotide excision repair |
ABCC1
|
−1.27 |
16p13.11 |
Involves in multi-drug resistance |
AP1S1
|
−1.09 |
7q22.1 |
Involves in endocytosis and Golgi processing |
APC
|
−1.19 |
5q22.2 |
Cell migration and adhesion |
ARNT
|
−1.05 |
1q21.3 |
Involves in xenobiotic metabolism |
BAX
|
−1.43 |
19q13.33 |
Involves in P53-mediated apoptosis |
BCL2
|
−1.14 |
18q21.33 |
In multiple transcript variants |
CDKN1A
|
−1.10 |
6p21.2 |
Interact with proliferating cell nuclear antigen, |
CDKN1B
|
−1.15 |
12p13.1 |
Controls the cell cycle progression |
CDKN2A
|
−1.13 |
9p21.3 |
Inhibits proliferation |
CDKN2D
|
−1.09 |
19p13.2 |
Participates in proliferation |
CYP1A1
|
−1.13 |
15q24.1 |
Involves in drug metabolism |
CYP1A2
|
−1.02 |
15q24.1 |
Involves in drug metabolism |
CYP2B6
|
−1.02 |
19q13.2 |
Involves in drug metabolism |
CYP2C9
|
−1.23 |
10q23.33 |
Involves in drug metabolism |
CYP2D6
|
−1.06 |
22q13.2 |
Involves in drug metabolism |
CYP3A4
|
−1.04 |
7q22.1 |
Involves in drug metabolism |
EPHX1
|
−1.25 |
1q42.12 |
Activation and detoxification of epoxides |
ERBB2
|
−1.27 |
17q12 |
Promotes cell proliferation |
ERBB3
|
−1.30 |
12q13.2 |
Promotes cell proliferation |
ERBB4
|
−1.23 |
2q34 |
Promotes cell proliferation |
ERCC3
|
−2.10 |
2q14.3 |
Nucleotide excision repair |
GAPDH
|
−1.08 |
Xq26.2-q26.3 |
Identified as a moonlighting protein |
GSK3A
|
−1.07 |
19q13.2 |
Regulates glycogen synthase and transcription factors |
GSTP1
|
−2.86 |
11q13.2 |
Reduces glutathione and detoxification |
HIF1A
|
−1.24 |
14q23.2 |
Involves in energy metabolism, angiogenesis, apoptosis |
IGF1R
|
−1.21 |
15q26.3 |
Enhances cell survival |
IGF2R
|
−1.12 |
6q25.3 |
Enhances cell survival |
MVP
|
−1.47 |
16p11.2 |
Participates in multiple cellular processes |
NFKB1
|
−1.02 |
4q24 |
Leads to cell development or delayed cell growth |
NFKBIB
|
−1.07 |
19q13.2 |
A transcription factor |
NFKBIE
|
−1.09 |
6p21.1 |
Promotes proliferation |
PPARD
|
−1.89 |
6p21.31 |
Inhibits the ligand-induced transcriptional activity |
RARA
|
−2.78 |
17q21.2 |
Implicated in regulation of development, differentiation, apoptosis |
RARG
|
−1.23 |
12q13.13 |
Involves in various biological processes |
RB1
|
−1.40 |
13q14.2 |
A negative regulator of the cell cycle |
RELB
|
−1.02 |
19q13.32 |
Activation in anti-inflammatory decidual endothelial cells |
RPLP0
|
−1.27 |
12q24.23 |
The functional equivalent of the E. coli L10 ribosomal protein |
RXRA
|
−1.71 |
9q34.2 |
Mediates the biological effects of retinoids |
RXRB
|
−1.19 |
6p21.32 |
Increases DNA binding |
SOD1
|
−1.10 |
21q22.11 |
A homodimer to convert naturally occuring |
TOP1
|
−1.28 |
20q12 |
Controls the topologic states of DNA during transcription. |
TOP2A
|
−1.11 |
17q21.2 |
Controls the topologic states of DNA during transcription. |
TOP2B
|
−1.32 |
3p24.2 |
Controls the topologic states of DNA during transcription. |
TP53
|
−1.08 |
17p13.1 |
Participates in cell cycle arrest, apoptosis, senescence, DNA repair |
TPMT
|
−1.19 |
6p22.3 |
Correlated with variations in sensitivity and toxicity |
XPC
|
−1.02 |
3p25.1 |
Plays an important role in the early steps of global genome nucleotide excision repair |