CNPY1

 

Full name: canopy FGF signaling regulator 1 Alias Symbol: 
Type: protein-coding gene Cytoband: 7q36.3
Entrez ID: 285888 HGNC ID: HGNC:27786 Ensembl Gene: ENSG00000146910 OMIM ID: 612493
Drug and gene relationship at DGIdb

 

Expression of CNPY1:

 

Dataset Gene EntrezID Probe Log2FC Adj.pValue Expression
GSE17351 CNPY1 285888 1559283_a_at -0.1040 0.6051
GSE26886 CNPY1 285888 1559283_a_at 0.0831 0.3550
GSE45670 CNPY1 285888 1559283_a_at -0.0065 0.9367
GSE53622 CNPY1 285888 118021 0.0247 0.8804
GSE53624 CNPY1 285888 118021 -0.0650 0.5034
GSE63941 CNPY1 285888 1559283_a_at 0.0447 0.7731
GSE77861 CNPY1 285888 1559283_a_at -0.0441 0.6262
GSE97050 CNPY1 285888 A_33_P3220347 0.2423 0.3710
TCGA CNPY1 285888 RNAseq 1.6711 0.1955

Upregulated datasets: 0; Downregulated datasets: 0.  


 

Survival by CNPY1 expression:

 

GSE53622GSE53624TCGA

 

Note: Click image to view full size file.  


Copy number change of CNPY1:

 

Dataset Gene EntrezID Gain Loss Normal Detail
GSE15526 CNPY1 285888 3 3 24
GSE20123 CNPY1 285888 2 3 25
GSE43470 CNPY1 285888 2 5 36
GSE46452 CNPY1 285888 7 2 50
GSE47630 CNPY1 285888 6 9 25
GSE54993 CNPY1 285888 3 3 64
GSE54994 CNPY1 285888 6 8 39
GSE60625 CNPY1 285888 0 0 11
GSE74703 CNPY1 285888 2 4 30
GSE74704 CNPY1 285888 0 3 17
TCGA CNPY1 285888 27 26 43

Total number of gains: 58; Total number of losses: 66; Total Number of normals: 364.  


 

Somatic mutations of CNPY1:

 

Generating mutation plots.

 

Highly correlated genes for CNPY1:

 

Showing top 20/173 corelated genes with mean PCC>0.5.
Gene1 Gene2 Mean PCC Num. Datasets Num. PCC<0 Num. PCC>0.5
CNPY1HCRT0.735638403
CNPY1FUZ0.731408303
CNPY1SSTR20.727365404
CNPY1FGF180.715391303
CNPY1LCN80.712571303
CNPY1PRSS380.710995303
CNPY1YY20.708158303
CNPY1DEFB1230.702132504
CNPY1KCNQ40.70199404
CNPY1PRSS540.697595303
CNPY1DRGX0.694925303
CNPY1DCD0.69138303
CNPY1STRC0.691222303
CNPY1BCL2L100.691113303
CNPY1TNFRSF140.69002303
CNPY1LDHAL6A0.686154303
CNPY1JAKMIP10.685427303
CNPY1MAT1A0.67598303
CNPY1OR2C10.675173504
CNPY1PRAMEF50.675097403

For details and further investigation, click here