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 
NTRK3ENSG00000140538  0.00    0.00    0    0  
CFBENSG00000243649  0.00    0.00    0    0  
SGK3ENSG00000104205  0.61    0.00    3    0  
KLHL17ENSG00000187961  0.00    0.82    0    4  
CYB5R4ENSG00000065615  0.00    0.12    0    1  
NISCHENSG00000010322  0.00    0.91    0    5  
CSNK1DENSG00000141551  0.80    0.21    4    2  
SMARCA4ENSG00000127616  0.00    0.00    0    0  
TMPRSS4ENSG00000137648  0.00    0.00    0    0  
DSCAMENSG00000171587  0.00    0.00    0    0  
KLHL15ENSG00000174010  0.30    0.00    2    0  
FREM1ENSG00000164946  0.00    0.00    0    0  
TFPIENSG00000003436  0.00    0.00    0    0  
CD80ENSG00000121594  0.00    0.00    0    0  
STK11ENSG00000118046  0.00    1.45    0    5  
FUCA1ENSG00000179163  0.00    1.81    0    5  
SFRP4ENSG00000106483  0.00    0.00    0    0  
CREBBPENSG00000005339  0.00    0.62    0    3  
CA11ENSG00000063180  0.00    0.56    0    2  
ATP8B2ENSG00000143515  0.22    0.00    1    0  

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