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 
TUFT1ENSG00000143367  1.92    0.00    7    0  
ALDH1A3ENSG00000184254  0.11    0.00    1    0  
CEACAM5ENSG00000105388  0.00    0.00    0    0  
ARID4AENSG00000032219  0.00    0.00    0    0  
HSD11B2ENSG00000176387  0.00    0.00    0    0  
NAPSAENSG00000131400  0.00    0.31    0    1  
MAP4K1ENSG00000104814  0.54    0.00    1    0  
PTPN14ENSG00000152104  0.00    0.39    0    2  
BCAT1ENSG00000060982  1.23    0.00    3    0  
ABCC3ENSG00000108846  0.00    0.00    0    0  
ADCYAP1R1ENSG00000078549  0.00    0.00    0    0  
MMP16ENSG00000156103  0.00    0.00    0    0  
GPC6ENSG00000183098  0.24    0.00    1    0  
LIPGENSG00000101670  0.00    0.00    0    0  
PASKENSG00000115687  0.00    1.45    0    7  
FLRT1ENSG00000126500  0.00    0.00    0    0  
BAMBIENSG00000095739  0.00    0.00    0    0  
LAMA3ENSG00000053747  0.15    0.00    1    0  
MATN3ENSG00000132031  0.18    0.15    1    1  
SCARB1ENSG00000073060  0.00    0.10    0    1  

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