Q-omics provides the consensus-scored RPS3AP43 profile across patient tissues and cancer cell-line models. RPS3AP43 expression is associated with patient survival in 19 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, RPS3AP43 is differentially expressed in 6, with the highest sampling consensus in LUSC. Additionally, RPS3AP43 RNA expression shows 11,426 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight ACC, LUSC, and UVM as cancer lineages where RPS3AP43 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.
Premium analyses for RPS3AP43 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RPS3AP43 survival associations across molecular data types. RPS3AP43 RNA expression shows survival associations in the most cancer types (19). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RPS3AP43 RNA expression–survival associations across cancer types. High RPS3AP43 expression shows unfavorable associations in ACC, but favorable associations in LGG, SKCM, LAML, LUSC and COAD. The ACC 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 ACC as the clearest survival context for RPS3AP43 RNA expression.
This table summarizes RPS3AP43 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 6. The strongest signals are observed in LUSC for RNA.
This table ranks reproducible tumor–normal expression differences for RPS3AP43. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RPS3AP43 shows lower tumor expression in LUSC and THCA and higher tumor expression in CHOL, READ, STAD and KIRC. The LUSC box plot shows higher RPS3AP43 RNA expression in normal versus tumor tissue (log2 FC = −0.160, t-test p = .002).
This table shows molecular features associated with RPS3AP43 in patient tissues and cancer cell lines. In patient samples, RPS3AP43 shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set.
