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 
HUNKENSG00000142149  0.00    0.00    0    0  
KCNC2ENSG00000166006  0.00    0.00    0    0  
MAPK6ENSG00000069956  0.00    0.10    0    1  
VARS2ENSG00000137411  0.00    0.00    0    0  
PHOSPHO1ENSG00000173868  0.00    0.00    0    0  
SLC28A3ENSG00000197506  0.00    0.00    0    0  
CLCN4ENSG00000073464  0.00    0.00    0    0  
PTPRKENSG00000152894  0.00    0.13    0    1  
SLC27A4ENSG00000167114  0.00    0.11    0    1  
GMPRENSG00000137198  0.00    0.00    0    0  
DNAJA1ENSG00000086061  0.00    0.00    0    0  
ICAM1ENSG00000090339  0.00    0.00    0    0  
SIDT2ENSG00000149577  0.00    1.05    0    5  
PRELPENSG00000188783  0.00    0.00    0    0  
FGF10ENSG00000070193  0.00    0.00    0    0  
ADGRL1ENSG00000072071  0.00    0.00    0    0  
PRIMPOLENSG00000164306  0.00    1.41    0    9  
SLCO3A1ENSG00000176463  0.18    0.00    1    0  
MBD5ENSG00000204406  0.00    0.30    0    2  
PTPDC1ENSG00000158079  0.00    0.00    0    0  

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