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 
EPAS1ENSG00000116016  0.00    0.00    0    0  
BRD9ENSG00000028310  2.81    0.13    9    1  
ADAM33ENSG00000149451  0.29    0.00    1    0  
RBKSENSG00000171174  0.16    0.00    1    0  
MASP1ENSG00000127241  0.00    0.00    0    0  
PPWD1ENSG00000113593  0.00    0.15    0    1  
PVRL4ENSG00000143217  1.16    0.00    2    0  
LOXL2ENSG00000134013  0.00    0.23    0    1  
SPNS3ENSG00000182557  0.00    0.12    0    1  
CLSTN1ENSG00000171603  0.00    2.06    0    6  
BMPR1BENSG00000138696  0.00    0.00    0    0  
EPHX1ENSG00000143819  0.11    0.24    1    1  
ALKENSG00000171094  0.00    0.00    0    0  
LGR5ENSG00000139292  0.00    0.00    0    0  
KCNJ15ENSG00000157551  0.00    0.00    0    0  
KLK4ENSG00000167749  0.23    0.00    1    0  
STAT6ENSG00000166888  0.12    0.00    1    0  
PTPRZ1ENSG00000106278  0.00    0.00    0    0  
LAMC2ENSG00000058085  0.00    0.00    0    0  
PLATENSG00000104368  0.44    0.00    1    0  

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