Q-omics provides the consensus-scored RPL4P3 profile across patient tissues and cancer cell-line models. RPL4P3 expression is associated with patient survival in 19 of 34 cancer types, with the highest sampling consensus in LUSC. Among the 18 cancer types available for tumor–normal comparison, RPL4P3 is differentially expressed in 10, with the highest sampling consensus in KIRC. Additionally, RPL4P3 RNA expression shows 13,130 significant gene co-expression associations, with the highest sampling consensus in ACC. Together, these results highlight LUSC, KIRC, and ACC as cancer lineages where RPL4P3 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 RPL4P3 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RPL4P3 survival associations across molecular data types. RPL4P3 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 RPL4P3 RNA expression–survival associations across cancer types. High RPL4P3 expression shows unfavorable associations in ACC and LIHC, but favorable associations in LUSC, SKCM, KIRC and BLCA. The LUSC Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p = .003). Together, the overview and detailed table identify LUSC as the clearest survival context for RPL4P3 RNA expression.
This table summarizes RPL4P3 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 10. The strongest signals are observed in KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for RPL4P3. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RPL4P3 shows lower tumor expression in BRCA and higher tumor expression in KIRC, COAD, LIHC, LUSC and READ. The KIRC box plot shows higher RPL4P3 RNA expression in tumor versus normal tissue (log2 FC = +0.365, t-test p < 0.001).
This table shows molecular features associated with RPL4P3 in patient tissues and cancer cell lines. In patient samples, RPL4P3 shows the broadest associations at the RNA and protein expression levels, with ACC recurring as the lineage with the largest associated feature set.
