Q-omics provides the consensus-scored RPS7P15 profile across patient tissues and cancer cell-line models. RPS7P15 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, RPS7P15 is differentially expressed in 7, with the highest sampling consensus in COAD. Additionally, RPS7P15 RNA expression shows 9,453 significant gene co-expression associations, with the highest sampling consensus in ACC. Together, these results highlight ACC, and COAD as cancer lineages where RPS7P15 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 RPS7P15 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RPS7P15 survival associations across molecular data types. RPS7P15 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 RPS7P15 RNA expression–survival associations across cancer types. High RPS7P15 expression shows unfavorable associations in ACC and CHOL, but favorable associations in CESC, LAML, LUSC and OV. 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 RPS7P15 RNA expression.
This table summarizes RPS7P15 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 COAD for RNA.
This table ranks reproducible tumor–normal expression differences for RPS7P15. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RPS7P15 shows lower tumor expression in THCA and higher tumor expression in COAD, HNSC, KICH, LUSC and STAD. The COAD box plot shows higher RPS7P15 RNA expression in tumor versus normal tissue (log2 FC = +0.733, t-test p < 0.001).
This table shows molecular features associated with RPS7P15 in patient tissues and cancer cell lines. In patient samples, RPS7P15 shows the broadest associations at the RNA and protein expression levels, with ACC recurring as the lineage with the largest associated feature set.
