Q-omics provides the consensus-scored RNY3P11 profile across patient tissues and cancer cell-line models. RNY3P11 expression is associated with patient survival in 15 of 34 cancer types, with the highest sampling consensus in KICH. Among the 18 cancer types available for tumor–normal comparison, RNY3P11 is differentially expressed in 2, with the highest sampling consensus in STAD. Additionally, RNY3P11 RNA expression shows 8,275 significant protein co-abundance associations, with the highest sampling consensus in HNSC. Together, these results highlight KICH, STAD, and HNSC as cancer lineages where RNY3P11 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 RNY3P11 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RNY3P11 survival associations across molecular data types. RNY3P11 RNA expression shows survival associations in the most cancer types (15). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RNY3P11 RNA expression–survival associations across cancer types. High RNY3P11 expression shows unfavorable associations in KICH, UCEC, LIHC and LAML, but favorable associations in UCS and STAD. The KICH 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 KICH as the clearest survival context for RNY3P11 RNA expression.
This table summarizes RNY3P11 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 2. The strongest signals are observed in STAD for RNA.
This table ranks reproducible tumor–normal expression differences for RNY3P11. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RNY3P11 shows higher tumor expression in STAD and LUSC. The STAD box plot shows higher RNY3P11 RNA expression in tumor versus normal tissue (log2 FC = +0.888, t-test p = .002).
This table shows molecular features associated with RNY3P11 in patient tissues and cancer cell lines. In patient samples, RNY3P11 shows the broadest associations at the RNA and protein expression levels, with HNSC recurring as the lineage with the largest associated feature set.
