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 
ICAM2ENSG00000108622  0.00    0.00    0    0  
FBN1ENSG00000166147  0.00    0.00    0    0  
FCRLAENSG00000132185  0.00    0.00    0    0  
PYGLENSG00000100504  0.00    0.00    0    0  
CNGB1ENSG00000070729  0.00    0.00    0    0  
MCOLN2ENSG00000153898  0.00    0.00    0    0  
ACTN4ENSG00000130402  0.55    0.11    1    1  
ZCWPW1ENSG00000078487  0.00    0.00    0    0  
SSH3ENSG00000172830  0.53    0.00    2    0  
NR1H3ENSG00000025434  0.00    0.00    0    0  
CPB2ENSG00000080618  0.00    0.00    0    0  
RORAENSG00000069667  0.00    0.00    0    0  
DPF3ENSG00000205683  0.00    0.11    0    1  
OBSCNENSG00000154358  0.14    0.23    1    1  
PTK2BENSG00000120899  0.00    0.51    0    4  
CYP46A1ENSG00000036530  0.00    0.00    0    0  
PLCB3ENSG00000149782  0.11    0.00    1    0  
NRXN3ENSG00000021645  0.00    0.22    0    2  
CERKENSG00000100422  0.00    0.64    0    4  
KCNC4ENSG00000116396  0.00    0.23    0    2  

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