Copy Number
The putative cancer-associated PDGs driven by SCNAs in each cancer type were identified by four criteria: 1) located in a peak region of a significantly recurrent focal SNCA locus estimated by the genomic identification of significant targets in cancer (GISTIC2) algorithm, (q≤0.25); 2) altered with high frequency and large amplitude (G-score ≥0.1); 3) mRNA reliably detected in at least 10% of tumor specimens in the given cancer type (90th percentile of FPKM value ≥1); and 4) mRNA significantly and positively correlated with copy numbers (Pearson P-value less than 0.001).
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Overall_Gscore | No. of Cancer Types | ||||
HGNC Symbol | Ensembl Gene ID | Amplification | Deletion | Amplification | Deletion |
PIGK | ENSG00000142892 | 0.00 | 0.00 | 0 | 0 |
SLC25A36 | ENSG00000114120 | 0.00 | 0.00 | 0 | 0 |
NPTN | ENSG00000156642 | 0.00 | 0.00 | 0 | 0 |
PRDM5 | ENSG00000138738 | 0.00 | 0.00 | 0 | 0 |
LPO | ENSG00000167419 | 0.00 | 0.00 | 0 | 0 |
LAP3 | ENSG00000002549 | 0.00 | 0.00 | 0 | 0 |
RHD | ENSG00000187010 | 0.00 | 0.00 | 0 | 0 |
SENP1 | ENSG00000079387 | 0.00 | 0.00 | 0 | 0 |
CRAT | ENSG00000095321 | 0.00 | 0.00 | 0 | 0 |
PDE11A | ENSG00000128655 | 0.00 | 0.00 | 0 | 0 |
MAPK8 | ENSG00000107643 | 0.00 | 0.00 | 0 | 0 |
GABRA2 | ENSG00000151834 | 0.00 | 0.00 | 0 | 0 |
CA1 | ENSG00000133742 | 0.00 | 0.00 | 0 | 0 |
SLC41A3 | ENSG00000114544 | 0.00 | 0.00 | 0 | 0 |
STK19 | ENSG00000204344 | 0.00 | 0.00 | 0 | 0 |
USP1 | ENSG00000162607 | 0.00 | 0.00 | 0 | 0 |
PHF8 | ENSG00000172943 | 0.00 | 0.00 | 0 | 0 |
SMYD5 | ENSG00000135632 | 0.00 | 0.00 | 0 | 0 |
ADAM10 | ENSG00000137845 | 0.00 | 0.00 | 0 | 0 |
PARP6 | ENSG00000137817 | 0.00 | 0.00 | 0 | 0 |
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