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 
SLC2A8ENSG00000136856  0.00    0.19    0    1  
CSNK1G3ENSG00000151292  0.25    0.13    1    1  
NEK4ENSG00000114904  0.00    0.71    0    4  
BRPF3ENSG00000096070  0.00    0.00    0    0  
ADAM18ENSG00000168619  0.00    0.00    0    0  
MAPK14ENSG00000112062  0.00    0.00    0    0  
NUCB1ENSG00000104805  0.00    0.52    0    2  
IMPA1ENSG00000133731  0.55    0.00    3    0  
HSD17B11ENSG00000198189  0.00    0.11    0    1  
CASKENSG00000147044  0.12    0.00    1    0  
KAT7ENSG00000136504  0.00    0.00    0    0  
CAMK2DENSG00000145349  0.00    0.00    0    0  
FKBP3ENSG00000100442  0.00    0.00    0    0  
SMPD1ENSG00000166311  0.00    0.00    0    0  
SPG7ENSG00000197912  0.00    0.92    0    6  
GFOD2ENSG00000141098  0.31    0.47    2    2  
MANBAENSG00000109323  0.00    0.13    0    1  
FKBP15ENSG00000119321  0.00    0.15    0    1  
ALCAMENSG00000170017  0.00    0.00    0    0  
BRD3ENSG00000169925  0.00    0.25    0    1  

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