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 
MGEA5ENSG00000198408  0.00    0.48    0    2  
CHID1ENSG00000177830  0.00    0.57    0    4  
A1BGENSG00000121410  0.00    0.35    0    1  
ATRNENSG00000088812  0.39    0.00    2    0  
PKN1ENSG00000123143  0.26    0.00    1    0  
NRD1ENSG00000078618  0.00    0.00    0    0  
ENTPD1ENSG00000138185  0.00    0.00    0    0  
CAPNS1ENSG00000126247  0.00    0.00    0    0  
ADCY6ENSG00000174233  0.00    0.00    0    0  
ATP4AENSG00000105675  0.00    0.00    0    0  
TRAP1ENSG00000126602  0.00    0.00    0    0  
SLC30A5ENSG00000145740  0.00    1.23    0    4  
KDM4AENSG00000066135  0.00    0.00    0    0  
PARP14ENSG00000173193  0.00    0.00    0    0  
PSAPENSG00000197746  0.00    0.00    0    0  
CELA2AENSG00000142615  0.00    0.00    0    0  
RHAGENSG00000112077  0.00    0.00    0    0  
SLC30A6ENSG00000152683  0.13    0.00    1    0  
HAT1ENSG00000128708  0.00    0.00    0    0  
RIOK3ENSG00000101782  0.13    0.00    1    0  

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