RPL21P116

associated omics data
Gene

Q-omics provides the consensus-scored RPL21P116 profile across patient tissues and cancer cell-line models. RPL21P116 expression is associated with patient survival in 22 of 34 cancer types, with the highest sampling consensus in OV. Among the 18 cancer types available for tumor–normal comparison, RPL21P116 is differentially expressed in 8, with the highest sampling consensus in KICH. Additionally, RPL21P116 RNA expression shows 9,054 significant gene co-expression associations, with the highest sampling consensus in SKCM. Together, these results highlight OV, KICH, and SKCM as cancer lineages where RPL21P116 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 RPL21P116 survival associations across molecular data types. RPL21P116 RNA expression shows survival associations in the most cancer types (22). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
RPL21P116 data typeSurvival analysisLineage consensusLineage of highest sampling consensus
RNAKaplan–Meier22OV (46)view →
This table ranks reproducible RPL21P116 RNA expression–survival associations across cancer types. High RPL21P116 expression shows unfavorable associations in OV, LUSC, UVM and ACC, but favorable associations in STAD and HNSC. The OV 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 OV as the clearest survival context for RPL21P116 RNA expression.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
OVOSQuartileII,III,IV0.5970.713.00146view →
LUSCDFSQuartileIII,IV0.2740.816.00812view →
UVMOSMedianIII,IV0.4680.931.00910view →
STADOSMedianIV0.5390.206.0119view →
ACCOSMedianIV0.4660.818.0119view →
HNSCDFSMedianIV0.5660.334.0219view →
Pink = unfavorable, green = favorable. all 22 lineages →

RPL21P116-OV (OS)

Kaplan–Meier survival curve for RPL21P116 RNA expression in OV: high vs low expression groups.

Explore this curve interactively →

Tumor vs Normal expression

This table summarizes RPL21P116 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 8. The strongest signals are observed in KICH for RNA.
RPL21P116 data typeExpression analysisLineage consensusLineage of highest sampling consensus
RNABox plot8KICH (9)view →
This table ranks reproducible tumor–normal expression differences for RPL21P116. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RPL21P116 shows lower tumor expression in KICH, LUSC and LUAD and higher tumor expression in COAD, KIRC and CHOL. The KICH box plot shows higher RPL21P116 RNA expression in normal versus tumor tissue (log2 FC = −0.252, t-test p < 0.001).
LineageGenderStageFold-changepSampling consensus
KICHMaleAll−0.252<.0019view →
COADMaleIII,IV+0.705.0028view →
KIRCAllAll+0.152<.0017view →
LUSCMaleAll−0.238<.0016view →
CHOLAllAll+0.422<.0015view →
LUADAllIII,IV−0.477.0044view →
Green = repressed in tumor. all 8 lineages →

RPL21P116-KICH

Tumor-vs-normal expression box plot for RPL21P116 in KICH.

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Cross-omics associations

This table shows molecular features associated with RPL21P116 in patient tissues and cancer cell lines. In patient samples, RPL21P116 shows the broadest associations at the RNA and protein expression levels, with SKCM recurring as the lineage with the largest associated feature set.
Associated data typeStrength (# associated data)Lineage of highest associated data
RNA
RNA9,054SKCM (1896)view →
Protein (mass-spec)8,728OV (1937)view →