Q-omics provides the consensus-scored RARRES2P7 profile across patient tissues and cancer cell-line models. RARRES2P7 expression is associated with patient survival in 14 of 34 cancer types, with the highest sampling consensus in STAD. Among the 18 cancer types available for tumor–normal comparison, RARRES2P7 is differentially expressed in 1, with the highest sampling consensus in LIHC. Additionally, RARRES2P7 RNA expression shows 4,697 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight STAD, and LIHC as cancer lineages where RARRES2P7 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 RARRES2P7 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RARRES2P7 survival associations across molecular data types. RARRES2P7 RNA expression shows survival associations in the most cancer types (14). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RARRES2P7 RNA expression–survival associations across cancer types. High RARRES2P7 expression shows unfavorable associations in STAD, KICH, UCEC, COAD, SKCM and UCS. The STAD 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 STAD as the clearest survival context for RARRES2P7 RNA expression.
This table summarizes RARRES2P7 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 1. The strongest signals are observed in LIHC for RNA.
This table ranks reproducible tumor–normal expression differences for RARRES2P7. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RARRES2P7 shows higher tumor expression in LIHC. The LIHC box plot shows higher RARRES2P7 RNA expression in tumor versus normal tissue (log2 FC = +0.127, t-test p = .045).
This table shows molecular features associated with RARRES2P7 in patient tissues and cancer cell lines. In patient samples, RARRES2P7 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
