Q-omics provides the consensus-scored RPS28P4 profile across patient tissues and cancer cell-line models. RPS28P4 expression is associated with patient survival in 25 of 34 cancer types, with the highest sampling consensus in UVM. Among the 18 cancer types available for tumor–normal comparison, RPS28P4 is differentially expressed in 7, with the highest sampling consensus in KIRC. Additionally, RPS28P4 RNA expression shows 17,200 significant gene co-expression associations, with the highest sampling consensus in THYM. Together, these results highlight UVM, KIRC, and THYM as cancer lineages where RPS28P4 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 RPS28P4 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RPS28P4 survival associations across molecular data types. RPS28P4 RNA expression shows survival associations in the most cancer types (25). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RPS28P4 RNA expression–survival associations across cancer types. High RPS28P4 expression shows unfavorable associations in LIHC, ACC and UCEC, but favorable associations in UVM, CESC and HNSC. The UVM Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p < 0.001). Together, the overview and detailed table identify UVM as the clearest survival context for RPS28P4 RNA expression.
This table summarizes RPS28P4 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 7. The strongest signals are observed in KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for RPS28P4. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RPS28P4 shows lower tumor expression in COAD and BRCA and higher tumor expression in KIRC, KIRP, LIHC and THCA. The KIRC box plot shows higher RPS28P4 RNA expression in tumor versus normal tissue (log2 FC = +1.009, t-test p < 0.001).
This table shows molecular features associated with RPS28P4 in patient tissues and cancer cell lines. In patient samples, RPS28P4 shows the broadest associations at the RNA and protein expression levels, with THYM recurring as the lineage with the largest associated feature set.
