FAM199X

 

Full name: family with sequence similarity 199, X-linked Alias Symbol: 
Type: protein-coding gene Cytoband: Xq22.2
Entrez ID: 139231 HGNC ID: HGNC:25195 Ensembl Gene: ENSG00000123575 OMIM ID: 
Drug and gene relationship at DGIdb

 

Expression of FAM199X:

 

Dataset Gene EntrezID Probe Log2FC Adj.pValue Expression
GSE17351 FAM199X 139231 225216_at -0.0862 0.8746
GSE26886 FAM199X 139231 227133_at -0.3993 0.1929
GSE45670 FAM199X 139231 227133_at 0.5835 0.0027
GSE53622 FAM199X 139231 68167 0.1194 0.0632
GSE53624 FAM199X 139231 68167 0.1148 0.0332
GSE63941 FAM199X 139231 227133_at 1.2414 0.0007
GSE77861 FAM199X 139231 225216_at 0.2393 0.2463
GSE97050 FAM199X 139231 A_23_P45294 -0.1314 0.7329
SRP007169 FAM199X 139231 RNAseq 0.0181 0.9648
SRP008496 FAM199X 139231 RNAseq 0.3361 0.1509
SRP064894 FAM199X 139231 RNAseq -0.0070 0.9748
SRP133303 FAM199X 139231 RNAseq 0.4920 0.0385
SRP159526 FAM199X 139231 RNAseq -0.1194 0.5488
SRP193095 FAM199X 139231 RNAseq -0.0965 0.3147
SRP219564 FAM199X 139231 RNAseq -0.0349 0.9141
TCGA FAM199X 139231 RNAseq 0.0110 0.8365

Upregulated datasets: 1; Downregulated datasets: 0.  


 

Survival by FAM199X expression:

 

GSE53622GSE53624TCGA

 

Note: Click image to view full size file.  


Copy number change of FAM199X:

 

No record found for this gene.


 

Somatic mutations of FAM199X:

 

Generating mutation plots.

 

Highly correlated genes for FAM199X:

 

Showing top 20/172 corelated genes with mean PCC>0.5.
Gene1 Gene2 Mean PCC Num. Datasets Num. PCC<0 Num. PCC>0.5
FAM199XPDE6D0.822317303
FAM199XLMBR10.782607303
FAM199XPIGA0.762982303
FAM199XFAM76B0.761946303
FAM199XKLHL110.758865303
FAM199XTPMT0.757009303
FAM199XAGBL50.754327303
FAM199XATG4C0.744747303
FAM199XMCM30.73653303
FAM199XZXDB0.736248303
FAM199XNKAP0.736208303
FAM199XFAM168A0.734017303
FAM199XMRPL380.732953303
FAM199XANKRD400.732749303
FAM199XSPRED20.730967303
FAM199XNCBP10.73303
FAM199XFCHSD20.72954303
FAM199XC17orf800.728841303
FAM199XZFX0.728016303
FAM199XRAC10.723721303

For details and further investigation, click here