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 
FBXL19ENSG00000099364  0.26    0.00    2    0  
BMPR1AENSG00000107779  0.00    0.00    0    0  
PDE3AENSG00000172572  0.00    0.00    0    0  
A2MENSG00000175899  0.00    0.00    0    0  
BMP2ENSG00000125845  0.00    0.00    0    0  
CETPENSG00000087237  0.00    0.00    0    0  
SLC16A12ENSG00000152779  0.00    0.00    0    0  
MBTPS1ENSG00000140943  0.00    0.79    0    4  
SECTM1ENSG00000141574  0.00    0.00    0    0  
CDK12ENSG00000167258  0.00    0.00    0    0  
COL27A1ENSG00000196739  0.00    0.00    0    0  
TDP1ENSG00000042088  0.00    0.51    0    2  
ACVR1ENSG00000115170  0.00    0.00    0    0  
DAPK2ENSG00000035664  0.00    0.00    0    0  
BCHEENSG00000114200  0.00    0.00    0    0  
KCNN4ENSG00000104783  0.00    0.00    0    0  
EPORENSG00000187266  0.00    0.00    0    0  
COL18A1ENSG00000182871  0.10    0.18    1    1  
LTFENSG00000012223  0.00    0.34    0    2  
TRPC6ENSG00000137672  0.00    0.00    0    0  

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