RPSAP54

associated omics data
Gene

Q-omics provides the consensus-scored RPSAP54 profile across patient tissues and cancer cell-line models. RPSAP54 expression is associated with patient survival in 28 of 34 cancer types, with the highest sampling consensus in LIHC. Among the 18 cancer types available for tumor–normal comparison, RPSAP54 is differentially expressed in 11, with the highest sampling consensus in COAD. Additionally, RPSAP54 RNA expression shows 16,176 significant gene co-expression associations, with the highest sampling consensus in ACC. Together, these results highlight LIHC, COAD, and ACC as cancer lineages where RPSAP54 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 RPSAP54 survival associations across molecular data types. RPSAP54 RNA expression shows survival associations in the most cancer types (28). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
RPSAP54 data typeSurvival analysisLineage consensusLineage of highest sampling consensus
RNAKaplan–Meier28LIHC (72)view →
This table ranks reproducible RPSAP54 RNA expression–survival associations across cancer types. High RPSAP54 expression shows unfavorable associations in LIHC, ACC, KICH and PAAD, but favorable associations in THCA and SKCM. The LIHC Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p < 0.001). Together, the overview and detailed table identify LIHC as the clearest survival context for RPSAP54 RNA expression.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
LIHCOSMedianAll0.5910.781<.00172view →
ACCDFSMedianAll0.2100.654<.00170view →
KICHDFSQuartileII,III,IV0.4121.000.00650view →
THCAOSQuartileAll1.0000.593.00342view →
PAADOSTertileAll0.2380.512<.00139view →
SKCMOSTertileIII,IV0.8210.501.00129view →
Pink = unfavorable, green = favorable. all 28 lineages →

RPSAP54-LIHC (OS)

Kaplan–Meier survival curve for RPSAP54 RNA expression in LIHC: high vs low expression groups.

Explore this curve interactively →

Tumor vs Normal expression

This table summarizes RPSAP54 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 11. The strongest signals are observed in COAD for RNA.
RPSAP54 data typeExpression analysisLineage consensusLineage of highest sampling consensus
RNABox plot11COAD (10)view →
This table ranks reproducible tumor–normal expression differences for RPSAP54. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RPSAP54 shows higher tumor expression in COAD, LIHC, STAD, KICH, THCA and CHOL. The COAD box plot shows higher RPSAP54 RNA expression in tumor versus normal tissue (log2 FC = +1.224, t-test p < 0.001).
LineageGenderStageFold-changepSampling consensus
COADFemaleII,III,IV+1.224<.00110view →
LIHCAllIII,IV+0.584<.0019view →
STADAllAll+0.451.0164view →
KICHMaleAll+0.455.0453view →
THCAFemaleII,III,IV+0.361.0013view →
CHOLAllAll+0.481<.0012view →
Green = repressed in tumor. all 11 lineages →

RPSAP54-COAD

Tumor-vs-normal expression box plot for RPSAP54 in COAD.

Explore this plot interactively →

Cross-omics associations

This table shows molecular features associated with RPSAP54 in patient tissues and cancer cell lines. In patient samples, RPSAP54 shows the broadest associations at the RNA and protein expression levels, with ACC recurring as the lineage with the largest associated feature set.
Associated data typeStrength (# associated data)Lineage of highest associated data
RNA
RNA16,176ACC (7171)view →
Function (RNA)7,048SKCM (2205)view →