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 
MPZENSG00000158887  0.10    0.00    1    0  
IFNAR2ENSG00000159110  0.00    0.00    0    0  
SV2AENSG00000159164  0.40    0.00    2    0  
LAD1ENSG00000159166  0.00    0.00    0    0  
STC1ENSG00000159167  0.00    0.00    0    0  
GIPENSG00000159224  0.00    0.00    0    0  
CBR1ENSG00000159228  0.00    0.00    0    0  
ATP13A2ENSG00000159363  0.00    0.79    0    4  
PSMB4ENSG00000159377  2.40    0.00    9    0  
CES5AENSG00000159398  0.00    0.00    0    0  
C1RENSG00000159403  0.00    0.00    0    0  
ALDH4A1ENSG00000159423  0.00    0.68    0    4  
PGLYRP3ENSG00000159527  0.00    0.00    0    0  
ATP6V0D1ENSG00000159720  0.30    0.18    2    1  
AGRPENSG00000159723  0.00    0.00    0    0  
LYPD5ENSG00000159871  0.00    0.29    0    1  
TNFRSF13CENSG00000159958  0.00    0.00    0    0  
OR3A3ENSG00000159961  0.00    0.00    0    0  
PTGIRENSG00000160013  0.00    0.00    0    0  
CALM3ENSG00000160014  0.14    0.51    1    2  

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