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 
MLXENSG00000108788  0.00    0.20    0    1  
CNTNAP1ENSG00000108797  0.00    0.00    0    0  
VAT1ENSG00000108828  0.00    0.00    0    0  
PPYENSG00000108849  0.00    0.00    0    0  
EFNB3ENSG00000108947  0.00    0.00    0    0  
FAM20AENSG00000108950  0.00    0.00    0    0  
DHRS7BENSG00000109016  0.17    0.19    1    1  
GABRA4ENSG00000109158  0.00    0.00    0    0  
GNRHRENSG00000109163  0.00    0.00    0    0  
UGT2B10ENSG00000109181  0.00    0.00    0    0  
SULT1E1ENSG00000109193  0.00    0.00    0    0  
ODAMENSG00000109205  0.00    0.00    0    0  
SMR3AENSG00000109208  0.00    0.00    0    0  
NMUENSG00000109255  0.62    0.00    2    0  
PF4V1ENSG00000109272  0.00    0.00    0    0  
AREGENSG00000109321  0.00    0.00    0    0  
UCP1ENSG00000109424  0.00    0.00    0    0  
IL2ENSG00000109471  0.00    0.00    0    0  
SOD3ENSG00000109610  0.00    0.00    0    0  
CPZENSG00000109625  0.00    0.00    0    0  

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