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 
IL17RCENSG00000163702  0.00    0.00    0    0  
TDRD7ENSG00000196116  0.00    0.00    0    0  
SLC35A5ENSG00000138459  0.00    0.00    0    0  
CDK17ENSG00000059758  0.00    0.00    0    0  
CACNG3ENSG00000006116  0.00    0.00    0    0  
VRK3ENSG00000105053  0.00    0.47    0    2  
ATP2C1ENSG00000017260  0.00    0.00    0    0  
SLC25A1ENSG00000100075  0.17    0.00    1    0  
CASP7ENSG00000165806  0.00    0.17    0    1  
ICKENSG00000112144  0.00    0.00    0    0  
PARLENSG00000175193  0.39    0.00    2    0  
PIK3R2ENSG00000105647  0.00    0.00    0    0  
LYG2ENSG00000185674  0.00    0.00    0    0  
ADCK4ENSG00000123815  0.00    0.11    0    1  
NPFFR1ENSG00000148734  0.00    0.00    0    0  
HTTENSG00000197386  0.00    0.00    0    0  
PRDM4ENSG00000110851  0.00    0.00    0    0  
CYP20A1ENSG00000119004  0.00    0.00    0    0  
STK38ENSG00000112079  0.00    0.00    0    0  
STK40ENSG00000196182  0.00    0.00    0    0  

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