Q-omics provides the consensus-scored RPS26P21 profile across patient tissues and cancer cell-line models. RPS26P21 expression is associated with patient survival in 17 of 34 cancer types, with the highest sampling consensus in BLCA. Among the 18 cancer types available for tumor–normal comparison, RPS26P21 is differentially expressed in 8, with the highest sampling consensus in LUSC. Additionally, RPS26P21 RNA expression shows 16,922 significant protein co-abundance associations, with the highest sampling consensus in LUAD. Together, these results highlight BLCA, LUSC, and LUAD as cancer lineages where RPS26P21 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 RPS26P21 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RPS26P21 survival associations across molecular data types. RPS26P21 RNA expression shows survival associations in the most cancer types (17). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RPS26P21 RNA expression–survival associations across cancer types. High RPS26P21 expression shows unfavorable associations in BLCA, KICH and LAML, but favorable associations in GBM, HNSC and LGG. The BLCA Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .010). Together, the overview and detailed table identify BLCA as the clearest survival context for RPS26P21 RNA expression.
This table summarizes RPS26P21 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 LUSC for RNA.
This table ranks reproducible tumor–normal expression differences for RPS26P21. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RPS26P21 shows lower tumor expression in LUSC, THCA, PAAD, LUAD and BRCA and higher tumor expression in READ. The LUSC box plot shows higher RPS26P21 RNA expression in normal versus tumor tissue (log2 FC = −0.538, t-test p < 0.001).
This table shows molecular features associated with RPS26P21 in patient tissues and cancer cell lines. In patient samples, RPS26P21 shows the broadest associations at the RNA and protein expression levels, with LUAD recurring as the lineage with the largest associated feature set.
