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 
TGENSG00000042832  0.37    0.00    2    0  
FGF9ENSG00000102678  0.00    0.22    0    1  
NOX4ENSG00000086991  0.00    0.00    0    0  
KLENSG00000133116  0.00    0.00    0    0  
RNASEH1ENSG00000171865  0.15    0.17    1    1  
KCNC3ENSG00000131398  0.23    0.32    1    1  
SPNS1ENSG00000169682  0.19    0.00    1    0  
CLCN2ENSG00000114859  0.39    0.10    2    1  
PMP2ENSG00000147588  0.00    0.00    0    0  
TMX2ENSG00000213593  0.00    0.11    0    1  
COL9A3ENSG00000092758  0.12    0.00    1    0  
KCNK2ENSG00000082482  0.00    0.16    0    1  
GRIK4ENSG00000149403  0.00    0.00    0    0  
GALK1ENSG00000108479  1.32    0.00    6    0  
MARK2ENSG00000072518  0.12    0.16    1    1  
HIPK1ENSG00000163349  0.00    0.49    0    3  
SERPINB7ENSG00000166396  0.00    0.00    0    0  
CELENSG00000170835  0.00    0.24    0    1  
PIK3R5ENSG00000141506  0.00    0.15    0    1  
HPENSG00000257017  0.00    0.00    0    0  

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