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 
PTGS2ENSG00000073756  0.00    0.00    0    0  
TSG101ENSG00000074319  0.00    0.00    0    0  
CA12ENSG00000074410  0.00    0.00    0    0  
MGLLENSG00000074416  0.00    0.00    0    0  
MYDGFENSG00000074842  0.00    0.71    0    1  
TUBE1ENSG00000074935  0.00    0.52    0    4  
TXKENSG00000074966  0.00    0.00    0    0  
TACR2ENSG00000075073  0.00    0.00    0    0  
WNT8BENSG00000075290  0.00    0.00    0    0  
SLC25A40ENSG00000075303  0.13    0.00    1    0  
FGF4ENSG00000075388  0.00    0.00    0    0  
CACNG5ENSG00000075429  0.00    0.00    0    0  
ATP12AENSG00000075673  0.00    0.00    0    0  
TUBA3DENSG00000075886  0.00    0.00    0    0  
SLC46A1ENSG00000076351  0.00    0.00    0    0  
MCAMENSG00000076706  0.00    0.12    0    1  
DNAJC10ENSG00000077232  0.12    0.00    1    0  
JADE1ENSG00000077684  0.00    0.00    0    0  
FKBP6ENSG00000077800  0.00    0.00    0    0  
CST7ENSG00000077984  0.00    0.00    0    0  

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