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 
CDKL3ENSG00000006837  0.28    0.00    1    0  
ADAM2ENSG00000104755  0.00    0.00    0    0  
MMP27ENSG00000137675  0.00    0.00    0    0  
MYH6ENSG00000197616  0.00    0.00    0    0  
TRPM5ENSG00000070985  0.00    0.00    0    0  
COLEC10ENSG00000184374  0.00    0.00    0    0  
PRDM12ENSG00000130711  0.00    0.00    0    0  
ADAM7ENSG00000069206  0.00    0.00    0    0  
CHRNA6ENSG00000147434  0.00    0.00    0    0  
LYZL1ENSG00000120563  0.00    0.00    0    0  
PZPENSG00000126838  0.00    0.00    0    0  
CGAENSG00000135346  0.00    0.00    0    0  
PSG1ENSG00000231924  0.00    0.00    0    0  
ESRRBENSG00000119715  0.00    0.00    0    0  
ABCA10ENSG00000154263  0.00    0.00    0    0  
CATSPER3ENSG00000152705  0.28    0.00    1    0  
TECTAENSG00000109927  0.00    0.00    0    0  
GABRR1ENSG00000146276  0.00    0.00    0    0  
SCN5AENSG00000183873  0.00    0.00    0    0  
TLL2ENSG00000095587  0.00    0.00    0    0  

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