RD3

 

Full name: retinal degeneration 3, GUCY2D regulator Alias Symbol: LCA12
Type: protein-coding gene Cytoband: 1q32.3
Entrez ID: 343035 HGNC ID: HGNC:19689 Ensembl Gene: ENSG00000198570 OMIM ID: 180040
Drug and gene relationship at DGIdb

 

Expression of RD3:

 

Dataset Gene EntrezID Probe Log2FC Adj.pValue Expression
GSE17351 RD3 343035 236563_at -0.2294 0.3120
GSE26886 RD3 343035 236563_at -0.0932 0.2212
GSE45670 RD3 343035 236563_at 0.0736 0.3660
GSE53622 RD3 343035 74131 -0.2279 0.2508
GSE53624 RD3 343035 74131 -0.7256 0.0002
GSE63941 RD3 343035 236563_at 0.0033 0.9837
GSE77861 RD3 343035 236563_at -0.0900 0.2144
SRP133303 RD3 343035 RNAseq 0.3784 0.1073
SRP193095 RD3 343035 RNAseq -0.1144 0.5458
TCGA RD3 343035 RNAseq -3.1301 0.0000

Upregulated datasets: 0; Downregulated datasets: 1.  


 

Survival by RD3 expression:

 

GSE53622GSE53624TCGA

 

Note: Click image to view full size file.  


Copy number change of RD3:

 

Dataset Gene EntrezID Gain Loss Normal Detail
GSE15526 RD3 343035 11 0 19
GSE20123 RD3 343035 10 0 20
GSE43470 RD3 343035 7 0 36
GSE46452 RD3 343035 3 1 55
GSE47630 RD3 343035 15 0 25
GSE54993 RD3 343035 0 6 64
GSE54994 RD3 343035 13 0 40
GSE60625 RD3 343035 0 0 11
GSE74703 RD3 343035 7 0 29
GSE74704 RD3 343035 4 0 16
TCGA RD3 343035 45 3 48

Total number of gains: 115; Total number of losses: 10; Total Number of normals: 363.  


 

Somatic mutations of RD3:

 

Generating mutation plots.

 

Highly correlated genes for RD3:

 

Showing top 20/73 corelated genes with mean PCC>0.5.
Gene1 Gene2 Mean PCC Num. Datasets Num. PCC<0 Num. PCC>0.5
RD3NAALADL10.697348303
RD3TPSD10.680009303
RD3GRHPR0.672566303
RD3EGFLAM-AS20.660262303
RD3COL14A10.643674303
RD3PRSS330.635533303
RD3FMN10.633034303
RD3ADH1B0.629583303
RD3RELN0.629544303
RD3SLCO2B10.628848303
RD3NME50.626941303
RD3KLK40.626675505
RD3TCL60.626545303
RD3HTR1E0.621838303
RD3SH3BGRL0.620522303
RD3S100B0.613107404
RD3ITM2A0.611178403
RD3LINC005890.610681303
RD3EBF30.610374303
RD3ARHGEF60.607344303

For details and further investigation, click here