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 
BMPR2ENSG00000204217  0.00    0.00    0    0  
INPP5EENSG00000148384  0.00    0.36    0    2  
NR1D1ENSG00000126368  0.00    0.00    0    0  
TCF20ENSG00000100207  0.00    0.23    0    1  
INSRRENSG00000027644  0.00    0.00    0    0  
PLAAENSG00000137055  0.00    0.25    0    2  
ADKENSG00000156110  0.00    0.00    0    0  
BAZ2AENSG00000076108  0.00    0.00    0    0  
ADAM9ENSG00000168615  0.00    0.00    0    0  
BPNT1ENSG00000162813  0.00    0.33    0    2  
CAPN15ENSG00000103326  0.00    0.33    0    2  
MAST3ENSG00000099308  0.00    0.00    0    0  
NEK1ENSG00000137601  0.00    0.00    0    0  
SLC41A1ENSG00000133065  0.12    0.00    1    0  
CORINENSG00000145244  0.00    0.00    0    0  
GNPTGENSG00000090581  0.00    0.31    0    2  
CALRENSG00000179218  0.14    0.00    1    0  
BOKENSG00000176720  0.00    1.90    0    7  
MAN2A2ENSG00000196547  0.59    0.00    3    0  
PRKXENSG00000183943  0.00    0.00    0    0  

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