Q-omics provides the consensus-scored RPS12P4 profile across patient tissues and cancer cell-line models. RPS12P4 expression is associated with patient survival in 23 of 34 cancer types, with the highest sampling consensus in OV. Among the 18 cancer types available for tumor–normal comparison, RPS12P4 is differentially expressed in 6, with the highest sampling consensus in COAD. Additionally, RPS12P4 RNA expression shows 9,455 significant protein co-abundance associations, with the highest sampling consensus in BRCA. Together, these results highlight OV, COAD, and BRCA as cancer lineages where RPS12P4 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 RPS12P4 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RPS12P4 survival associations across molecular data types. RPS12P4 RNA expression shows survival associations in the most cancer types (23). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RPS12P4 RNA expression–survival associations across cancer types. High RPS12P4 expression shows unfavorable associations in OV, ACC and KICH, but favorable associations in READ, LUAD and CESC. The OV Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .005). Together, the overview and detailed table identify OV as the clearest survival context for RPS12P4 RNA expression.
This table summarizes RPS12P4 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 COAD for RNA.
This table ranks reproducible tumor–normal expression differences for RPS12P4. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RPS12P4 shows lower tumor expression in THCA and BLCA and higher tumor expression in COAD, LUAD, PRAD and READ. The COAD box plot shows higher RPS12P4 RNA expression in tumor versus normal tissue (log2 FC = +0.591, t-test p = .001).
This table shows molecular features associated with RPS12P4 in patient tissues and cancer cell lines. In patient samples, RPS12P4 shows the broadest associations at the RNA and protein expression levels, with BRCA recurring as the lineage with the largest associated feature set.
