Q-omics provides the consensus-scored RAD23BP2 profile across patient tissues and cancer cell-line models. RAD23BP2 expression is associated with patient survival in 11 of 34 cancer types, with the highest sampling consensus in READ. Among the 18 cancer types available for tumor–normal comparison, RAD23BP2 is differentially expressed in 1, with the highest sampling consensus in LUAD. Additionally, RAD23BP2 RNA expression shows 6,054 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight READ, LUAD, and STAD as cancer lineages where RAD23BP2 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 RAD23BP2 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RAD23BP2 survival associations across molecular data types. RAD23BP2 RNA expression shows survival associations in the most cancer types (11). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RAD23BP2 RNA expression–survival associations across cancer types. High RAD23BP2 expression shows unfavorable associations in READ, KIRP, BRCA, LUSC, THCA and STAD. The READ 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 READ as the clearest survival context for RAD23BP2 RNA expression.
This table summarizes RAD23BP2 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 LUAD for RNA.
This table ranks reproducible tumor–normal expression differences for RAD23BP2. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RAD23BP2 shows higher tumor expression in LUAD. The LUAD box plot shows higher RAD23BP2 RNA expression in tumor versus normal tissue (log2 FC = +0.010, t-test p = .025).
This table shows molecular features associated with RAD23BP2 in patient tissues and cancer cell lines. In patient samples, RAD23BP2 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
