C19orf81

 

Full name: chromosome 19 open reading frame 81 Alias Symbol: 
Type: protein-coding gene Cytoband: 19q13.33
Entrez ID: 342918 HGNC ID: HGNC:40041 Ensembl Gene: ENSG00000235034 OMIM ID: 
Drug and gene relationship at DGIdb

 

Expression of C19orf81:

 

Dataset Gene EntrezID Probe Log2FC Adj.pValue Expression
GSE17351 C19orf81 342918 230814_at 0.0621 0.8291
GSE26886 C19orf81 342918 230814_at 0.4463 0.0062
GSE45670 C19orf81 342918 230814_at 0.0341 0.7516
GSE63941 C19orf81 342918 230814_at 0.2702 0.0774
GSE77861 C19orf81 342918 230814_at 0.0549 0.7302
GSE97050 C19orf81 A_21_P0000121 -0.0896 0.7831
SRP159526 C19orf81 342918 RNAseq 1.3483 0.0343
SRP219564 C19orf81 342918 RNAseq 0.6037 0.3559

Upregulated datasets: 1; Downregulated datasets: 0.  


 

Copy number change of C19orf81:

 

Dataset Gene EntrezID Gain Loss Normal Detail
GSE15526 C19orf81 342918 3 4 23
GSE20123 C19orf81 342918 3 3 24
GSE43470 C19orf81 342918 4 11 28
GSE46452 C19orf81 342918 45 1 13
GSE47630 C19orf81 342918 10 6 24
GSE54993 C19orf81 342918 17 4 49
GSE54994 C19orf81 342918 4 14 35
GSE60625 C19orf81 342918 9 0 2
GSE74703 C19orf81 342918 4 7 25
GSE74704 C19orf81 342918 3 1 16
TCGA C19orf81 342918 14 19 63

Total number of gains: 116; Total number of losses: 70; Total Number of normals: 302.  


 

Somatic mutations of C19orf81:

 

Generating mutation plots.

 

Highly correlated genes for C19orf81:

 

Showing top 20/225 corelated genes with mean PCC>0.5.
Gene1 Gene2 Mean PCC Num. Datasets Num. PCC<0 Num. PCC>0.5
C19orf81NAT8B0.846685303
C19orf81MAG0.803167303
C19orf81ADAMTS70.793637303
C19orf81GNL10.790824303
C19orf81GPR1500.786118303
C19orf81EVX10.783906404
C19orf81CDRT150.775033303
C19orf81TMEM151B0.772481303
C19orf81GRIN10.770137303
C19orf81FUT70.76203404
C19orf81BIRC70.757685303
C19orf81GCM20.756655303
C19orf81PNMA6A0.755304303
C19orf81CCDC570.753952303
C19orf81DPYSL40.749088303
C19orf81DUSP90.746607303
C19orf81PCSK1N0.742214303
C19orf81RCOR20.738927303
C19orf81LAMTOR20.738207303
C19orf81GRAP0.736401303

For details and further investigation, click here