Q-omics provides the consensus-scored RNY1P10 profile across patient tissues and cancer cell-line models. RNY1P10 expression is associated with patient survival in 12 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, RNY1P10 is differentially expressed in 5, with the highest sampling consensus in THCA. Additionally, RNY1P10 RNA expression shows 6,577 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight KIRC, THCA, and STAD as cancer lineages where RNY1P10 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 RNY1P10 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RNY1P10 survival associations across molecular data types. RNY1P10 RNA expression shows survival associations in the most cancer types (12). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RNY1P10 RNA expression–survival associations across cancer types. High RNY1P10 expression shows unfavorable associations in KIRC, UCS, COAD and SKCM, but favorable associations in LUAD and HNSC. The KIRC 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 KIRC as the clearest survival context for RNY1P10 RNA expression.
This table summarizes RNY1P10 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 5. The strongest signals are observed in THCA for RNA.
This table ranks reproducible tumor–normal expression differences for RNY1P10. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RNY1P10 shows lower tumor expression in THCA, BRCA and LUSC and higher tumor expression in STAD and ESCA. The THCA box plot shows higher RNY1P10 RNA expression in normal versus tumor tissue (log2 FC = −0.487, t-test p < 0.001).
This table shows molecular features associated with RNY1P10 in patient tissues and cancer cell lines. In patient samples, RNY1P10 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
