Q-omics provides the consensus-scored RRAS2P2 profile across patient tissues and cancer cell-line models. RRAS2P2 expression is associated with patient survival in 10 of 34 cancer types, with the highest sampling consensus in COAD. Among the 18 cancer types available for tumor–normal comparison, RRAS2P2 is differentially expressed in 4, with the highest sampling consensus in LUAD. Additionally, RRAS2P2 RNA expression shows 6,251 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight COAD, LUAD, and STAD as cancer lineages where RRAS2P2 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 RRAS2P2 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RRAS2P2 survival associations across molecular data types. RRAS2P2 RNA expression shows survival associations in the most cancer types (10). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RRAS2P2 RNA expression–survival associations across cancer types. High RRAS2P2 expression shows unfavorable associations in COAD, ESCA, LUSC and LUAD, but favorable associations in BRCA and GBM. The COAD Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .003). Together, the overview and detailed table identify COAD as the clearest survival context for RRAS2P2 RNA expression.
This table summarizes RRAS2P2 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 4. The strongest signals are observed in LUSC for RNA.
This table ranks reproducible tumor–normal expression differences for RRAS2P2. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RRAS2P2 shows lower tumor expression in LUAD, LUSC and PAAD and higher tumor expression in UCEC. The LUAD box plot shows higher RRAS2P2 RNA expression in normal versus tumor tissue (log2 FC = −0.078, t-test p = .004).
This table shows molecular features associated with RRAS2P2 in patient tissues and cancer cell lines. In patient samples, RRAS2P2 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
