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 
GPR6ENSG00000146360  0.00    0.00    0    0  
TAAR2ENSG00000146378  0.00    0.00    0    0  
TAAR6ENSG00000146383  0.00    0.00    0    0  
TAAR8ENSG00000146385  0.00    0.00    0    0  
TAAR1ENSG00000146399  0.00    0.00    0    0  
VIPENSG00000146469  0.00    0.00    0    0  
IGFBP1ENSG00000146678  0.00    0.00    0    0  
SSC4DENSG00000146700  0.00    0.00    0    0  
SLC12A9ENSG00000146828  0.00    0.00    0    0  
TMEM27ENSG00000147003  0.00    0.00    0    0  
SPIN2AENSG00000147059  0.00    0.00    0    0  
HDAC8ENSG00000147099  0.00    0.00    0    0  
GPR174ENSG00000147138  0.00    0.00    0    0  
EBPENSG00000147155  0.00    0.00    0    0  
IL2RGENSG00000147168  0.00    0.00    0    0  
GPR119ENSG00000147262  0.00    0.00    0    0  
NSDHLENSG00000147383  0.42    0.00    3    0  
GNRH1ENSG00000147437  0.00    0.49    0    3  
SLC25A37ENSG00000147454  0.00    0.91    0    6  
CRHENSG00000147571  0.00    0.00    0    0  

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