Q-omics provides the consensus-scored STAU2P1 profile across patient tissues and cancer cell-line models. STAU2P1 expression is associated with patient survival in 14 of 34 cancer types, with the highest sampling consensus in UVM. Among the 18 cancer types available for tumor–normal comparison, STAU2P1 is differentially expressed in 2, with the highest sampling consensus in LUAD. Additionally, STAU2P1 RNA expression shows 5,989 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight UVM, LUAD, and STAD as cancer lineages where STAU2P1 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 STAU2P1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes STAU2P1 survival associations across molecular data types. STAU2P1 RNA expression shows survival associations in the most cancer types (14), followed by mutation status (1). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible STAU2P1 RNA expression–survival associations across cancer types. High STAU2P1 expression shows unfavorable associations in UVM, MESO, KIRC, BLCA and THCA, but favorable associations in UCS. The UVM Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .004). Together, the overview and detailed table identify UVM as the clearest survival context for STAU2P1 RNA expression.
This table summarizes STAU2P1 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 LUAD for RNA.
This table ranks reproducible tumor–normal expression differences for STAU2P1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. STAU2P1 shows higher tumor expression in LUAD and HNSC. The LUAD box plot shows higher STAU2P1 RNA expression in tumor versus normal tissue (log2 FC = +0.060, t-test p = .030).
This table shows molecular features associated with STAU2P1 in patient tissues and cancer cell lines. In patient samples, STAU2P1 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
