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 
ATG4BENSG00000168397  0.00    2.47    0    10  
SFTPDENSG00000133661  0.00    0.00    0    0  
ROR2ENSG00000169071  0.00    0.00    0    0  
ABCC1ENSG00000103222  0.00    0.00    0    0  
PHEXENSG00000102174  0.00    0.00    0    0  
CPDENSG00000108582  0.00    0.00    0    0  
CHRNA9ENSG00000174343  0.00    0.00    0    0  
ITGA5ENSG00000161638  0.00    0.00    0    0  
CYP2S1ENSG00000167600  0.00    0.00    0    0  
PRKAR1BENSG00000188191  0.54    0.41    4    1  
AMPD3ENSG00000133805  0.00    0.00    0    0  
ADAMTS6ENSG00000049192  0.00    0.00    0    0  
SLC9B2ENSG00000164038  0.00    0.13    0    1  
GANCENSG00000214013  0.00    0.84    0    5  
CARD17ENSG00000255221  0.00    0.00    0    0  
PLA1AENSG00000144837  0.00    0.00    0    0  
ACACAENSG00000278540  0.00    0.00    0    0  
CDC14BENSG00000081377  0.00    0.00    0    0  
SLC47A2ENSG00000180638  0.00    0.00    0    0  
AQP9ENSG00000103569  0.00    0.00    0    0  

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