Table 1.
Probe-set ID | P-value | Fold change (T vs N) | Gene symbol | Entrez Gene ID | Chromosomal location | UniGene ID |
---|---|---|---|---|---|---|
204705_x_at | 0.001758 | 0.14098111 | ALDOB | 229 | chr9q21.3-q22.2 | Hs.530274 |
206461_x_at | 5.55E-06 | 0.19372810 | MT1H | 4496 | chr16q13 | Hs.438462 |
213953_at | 0.001642 | 0.24914121 | KRT20 | 54474 | chr17q21.2 | Hs.84905 |
241981_at | 0.000162 | 0.25906518 | FAM20A | 54757 | chr17q24.2 | Hs.268874 |
227948_at | 9.90E-06 | 0.28067371 | FGD4 | 121512 | chr12p11.21 | Hs.117835 |
215563_s_at | 0.00418 | 0.30904312 | MST1P9 | 11223 | chr1p36.13 | Hs.655432 |
201348_at | 0.000617 | 0.33314741 | GPX3 | 2878 | chr5q23 | Hs.723871 |
214235_at | 0.001145 | 0.33344691 | CYP3A5 | 1577 | chr7q21.1 | Hs.695915 |
209894_at | 0.042845 | 0.36366159 | LEPR | 3953 | chr1p31 | Hs.723178 |
207017_at | 0.005814 | 0.37384713 | RAB27B | 5874 | chr18q21.2 | Hs.25318 |
205112_at | 0.000528 | 0.38194046 | PLCE1 | 51196 | chr10q23 | Hs.655033 |
211470_s_at | 0.007601 | 0.38232091 | SULT1C2 | 6819 | chr2q12.3 | Hs.436123 |
1559706_at | 0.002404 | 0.40676872 | RGNEF | 64283 | chr5q13.2 | Hs.482521 |
207222_at | 0.005203 | 0.40781420 | PLA2G10 | 8399 | chr16p13.1-p12 | Hs.567366 |
Notes: P-values were based on student’s t-test. A difference was considered significant when P<0.05.
Abbreviations: T, tumor tissue; N, nontumor tissue.