Q-omics provides the consensus-scored UBE2Q2P11 profile across patient tissues and cancer cell-line models. UBE2Q2P11 expression is associated with patient survival in 12 of 34 cancer types, with the highest sampling consensus in THCA. Among the 18 cancer types available for tumor–normal comparison, UBE2Q2P11 is differentially expressed in 5, with the highest sampling consensus in KICH. Additionally, UBE2Q2P11 RNA expression shows 6,091 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight THCA, KICH, and STAD as cancer lineages where UBE2Q2P11 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 UBE2Q2P11 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes UBE2Q2P11 survival associations across molecular data types. UBE2Q2P11 RNA expression shows survival associations in the most cancer types (12). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible UBE2Q2P11 RNA expression–survival associations across cancer types. High UBE2Q2P11 expression shows unfavorable associations in THCA, STAD, TGCT, KIRC and COAD, but favorable associations in UCS. The THCA 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 THCA as the clearest survival context for UBE2Q2P11 RNA expression.
This table summarizes UBE2Q2P11 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 5. The strongest signals are observed in KICH for RNA.
This table ranks reproducible tumor–normal expression differences for UBE2Q2P11. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. UBE2Q2P11 shows lower tumor expression in UCEC, PRAD and STAD and higher tumor expression in KICH and KIRP. The KICH box plot shows higher UBE2Q2P11 RNA expression in tumor versus normal tissue (log2 FC = +0.136, t-test p = .008).
This table shows molecular features associated with UBE2Q2P11 in patient tissues and cancer cell lines. In patient samples, UBE2Q2P11 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
