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).

 

Pan-cancer level overall G-score of PDGs that recurrently gained or lost copy number in at least one cancer types


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Overall_Gscore No. of Cancer Types
 HGNC Symbol  Ensembl Gene ID  Amplification  Deletion  Amplification  Deletion 
PIGKENSG00000142892  0.00    0.00    0    0  
SLC25A36ENSG00000114120  0.00    0.00    0    0  
NPTNENSG00000156642  0.00    0.00    0    0  
PRDM5ENSG00000138738  0.00    0.00    0    0  
LPOENSG00000167419  0.00    0.00    0    0  
LAP3ENSG00000002549  0.00    0.00    0    0  
RHDENSG00000187010  0.00    0.00    0    0  
SENP1ENSG00000079387  0.00    0.00    0    0  
CRATENSG00000095321  0.00    0.00    0    0  
PDE11AENSG00000128655  0.00    0.00    0    0  
MAPK8ENSG00000107643  0.00    0.00    0    0  
GABRA2ENSG00000151834  0.00    0.00    0    0  
CA1ENSG00000133742  0.00    0.00    0    0  
SLC41A3ENSG00000114544  0.00    0.00    0    0  
STK19ENSG00000204344  0.00    0.00    0    0  
USP1ENSG00000162607  0.00    0.00    0    0  
PHF8ENSG00000172943  0.00    0.00    0    0  
SMYD5ENSG00000135632  0.00    0.00    0    0  
ADAM10ENSG00000137845  0.00    0.00    0    0  
PARP6ENSG00000137817  0.00    0.00    0    0  

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