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 
PI4KAENSG00000241973  0.58    0.00    2    0  
PIK3C3ENSG00000078142  0.00    0.00    0    0  
CAMK4ENSG00000152495  0.00    0.14    0    1  
THBS2ENSG00000186340  0.00    0.00    0    0  
ATP6V1AENSG00000114573  0.00    0.00    0    0  
BLMENSG00000197299  0.73    0.00    4    0  
SLC39A6ENSG00000141424  0.00    0.00    0    0  
SETD2ENSG00000181555  0.00    0.71    0    4  
SMYD3ENSG00000185420  0.90    0.25    4    1  
SLC44A4ENSG00000204385  0.00    0.00    0    0  
F12ENSG00000131187  0.00    0.11    0    1  
SRMENSG00000116649  0.11    0.64    1    3  
CHD7ENSG00000171316  0.36    0.00    2    0  
PDK1ENSG00000152256  0.00    0.00    0    0  
TP53ENSG00000141510  0.00    1.12    0    3  
PLD1ENSG00000075651  1.15    0.00    3    0  
EPCAMENSG00000119888  0.13    0.00    1    0  
FAT1ENSG00000083857  0.00    1.49    0    7  
NEGR1ENSG00000172260  0.00    0.00    0    0  
CD3GENSG00000160654  0.00    0.23    0    1  

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