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 
SLC37A3ENSG00000157800  0.34    0.14    2    1  
RDH11ENSG00000072042  0.00    0.84    0    4  
CFLARENSG00000003402  0.14    0.00    1    0  
COL4A3ENSG00000169031  0.00    0.19    0    1  
PHF12ENSG00000109118  0.29    0.00    1    0  
DPEP2ENSG00000167261  0.00    0.00    0    0  
ADORA2BENSG00000170425  0.00    0.12    0    1  
GPLD1ENSG00000112293  0.00    0.00    0    0  
PPATENSG00000128059  0.62    0.00    3    0  
HTRA4ENSG00000169495  0.00    0.00    0    0  
ZRANB3ENSG00000121988  0.00    0.19    0    1  
AMBPENSG00000106927  0.00    0.00    0    0  
EFNA4ENSG00000243364  1.54    0.00    6    0  
AKR1B10ENSG00000198074  0.00    0.00    0    0  
CACNB1ENSG00000067191  0.00    0.00    0    0  
IL17BENSG00000127743  0.00    0.00    0    0  
RAI1ENSG00000108557  0.76    0.16    1    1  
MAOAENSG00000189221  0.00    0.00    0    0  
ABCA2ENSG00000107331  0.28    0.52    2    3  
NR0B1ENSG00000169297  0.00    0.00    0    0  

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