RP2

 

Full name: RP2 activator of ARL3 GTPase Alias Symbol: TBCCD2|NME10|NM23-H10
Type: protein-coding gene Cytoband: Xp11.3
Entrez ID: 6102 HGNC ID: HGNC:10274 Ensembl Gene: ENSG00000102218 OMIM ID: 300757
Drug and gene relationship at DGIdb

 

Expression of RP2:

 

Dataset Gene EntrezID Probe Log2FC Adj.pValue Expression
GSE17351 RP2 6102 205191_at -0.5723 0.4079
GSE20347 RP2 6102 205191_at -1.1629 0.0000
GSE23400 RP2 6102 205191_at -0.0789 0.1594
GSE26886 RP2 6102 205191_at -0.9941 0.0003
GSE29001 RP2 6102 205191_at -0.9958 0.0230
GSE38129 RP2 6102 205191_at -0.6697 0.0010
GSE45670 RP2 6102 205191_at -0.4849 0.0807
GSE53622 RP2 6102 73038 -0.8714 0.0000
GSE53624 RP2 6102 73038 -0.8141 0.0000
GSE63941 RP2 6102 205191_at -2.0654 0.0022
GSE77861 RP2 6102 205191_at -0.7055 0.0240
GSE97050 RP2 6102 A_23_P22433 -0.2079 0.4566
SRP007169 RP2 6102 RNAseq -0.4516 0.1844
SRP008496 RP2 6102 RNAseq -0.3510 0.1397
SRP064894 RP2 6102 RNAseq -0.8386 0.0214
SRP133303 RP2 6102 RNAseq 0.1112 0.7244
SRP159526 RP2 6102 RNAseq -0.6203 0.1229
SRP193095 RP2 6102 RNAseq -0.8233 0.0000
SRP219564 RP2 6102 RNAseq -0.7699 0.1173
TCGA RP2 6102 RNAseq -0.0343 0.5911

Upregulated datasets: 0; Downregulated datasets: 2.  


 

Survival by RP2 expression:

 

GSE53622GSE53624TCGA

 

Note: Click image to view full size file.  


Copy number change of RP2:

 

No record found for this gene.


 

Somatic mutations of RP2:

 

Generating mutation plots.

 

Highly correlated genes for RP2:

 

Showing top 20/624 corelated genes with mean PCC>0.5.
Gene1 Gene2 Mean PCC Num. Datasets Num. PCC<0 Num. PCC>0.5
RP2C15orf480.70547606
RP2ORMDL20.68566403
RP2PGM20.68275505
RP2CXCR20.682525909
RP2GSKIP0.680071505
RP2EBPL0.673935303
RP2TMOD30.6730641008
RP2RAB100.670519605
RP2ALDH9A10.67002210010
RP2ULK30.667908504
RP2DNTT0.666021303
RP2KAT2B0.66586110010
RP2CAST0.662244908
RP2C3orf380.65499504
RP2SOCS60.654823807
RP2GRPEL20.653859505
RP2DEGS20.652341505
RP2PRR15L0.648329505
RP2SLC25A510.64509403
RP2RASSF50.644563606

For details and further investigation, click here