RAC1P5

associated omics data
Gene

Q-omics provides the consensus-scored RAC1P5 profile across patient tissues and cancer cell-line models. RAC1P5 expression is associated with patient survival in 21 of 34 cancer types, with the highest sampling consensus in LIHC. Among the 18 cancer types available for tumor–normal comparison, RAC1P5 is differentially expressed in 5, with the highest sampling consensus in BRCA. Additionally, RAC1P5 RNA expression shows 8,413 significant protein co-abundance associations, with the highest sampling consensus in OV. Together, these results highlight LIHC, BRCA, and OV as cancer lineages where RAC1P5 shows reproducible signals across survival, tumor–normal expression, and patient cross-omics analyses.

Every result is evaluated using two consensus scores. Sampling consensus measures how consistently a finding is reproduced within a cancer lineage across different conditions. Lineage consensus measures how broadly the result is shared across cancer types, distinguishing pan-cancer signals from lineage-specific patterns.

Survival associations

This table summarizes RAC1P5 survival associations across molecular data types. RAC1P5 RNA expression shows survival associations in the most cancer types (21). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
RAC1P5 data typeSurvival analysisLineage consensusLineage of highest sampling consensus
RNAKaplan–Meier21LIHC (39)view →
This table ranks reproducible RAC1P5 RNA expression–survival associations across cancer types. High RAC1P5 expression shows unfavorable associations in LIHC, COAD and UCEC, but favorable associations in LUSC, CESC and KIRC. The LIHC Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .001). Together, the overview and detailed table identify LIHC as the clearest survival context for RAC1P5 RNA expression.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
LIHCOSQuartileAll0.3390.556.00139view →
LUSCOSTertileII,III,IV0.7200.558.01136view →
CESCDFSQuartileAll0.8350.644.00634view →
COADOSQuartileAll0.5100.724.00629view →
KIRCDFSTertileIV0.9170.434<.00126view →
UCECDFSMedianAll0.6210.667.01224view →
Pink = unfavorable, green = favorable. all 21 lineages →

RAC1P5-LIHC (OS)

Kaplan–Meier survival curve for RAC1P5 RNA expression in LIHC: high vs low expression groups.

Explore this curve interactively →

Tumor vs Normal expression

This table summarizes RAC1P5 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 5. The strongest signals are observed in BRCA for RNA.
RAC1P5 data typeExpression analysisLineage consensusLineage of highest sampling consensus
RNABox plot5BRCA (4)view →
This table ranks reproducible tumor–normal expression differences for RAC1P5. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RAC1P5 shows lower tumor expression in PAAD and LIHC and higher tumor expression in BRCA, HNSC, LUSC and LIHC. The BRCA box plot shows higher RAC1P5 RNA expression in tumor versus normal tissue (log2 FC = +0.051, t-test p = .018).
LineageGenderStageFold-changepSampling consensus
BRCAFemaleII,III,IV+0.051.0184view →
PAADFemaleAll−0.229.0072view →
HNSCFemaleIV+0.150.0112view →
LUSCMaleAll+0.083.0092view →
LIHCFemaleIII,IV−0.136.0041view →
LIHCMaleAll+0.044.0251view →
Green = repressed in tumor. all 5 lineages →

RAC1P5-BRCA

Tumor-vs-normal expression box plot for RAC1P5 in BRCA.

Explore this plot interactively →

Cross-omics associations

This table shows molecular features associated with RAC1P5 in patient tissues and cancer cell lines. In patient samples, RAC1P5 shows the broadest associations at the RNA and protein expression levels, with OV recurring as the lineage with the largest associated feature set.
Associated data typeStrength (# associated data)Lineage of highest associated data
RNA
Protein (mass-spec)8,413OV (2123)view →
RNA5,846KICH (1753)view →