Q-omics provides the consensus-scored COP1P1 profile across patient tissues and cancer cell-line models. COP1P1 expression is associated with patient survival in 15 of 34 cancer types, with the highest sampling consensus in STAD. Among the 18 cancer types available for tumor–normal comparison, COP1P1 is differentially expressed in 6, with the highest sampling consensus in KIRC. Additionally, COP1P1 RNA expression shows 11,618 significant protein co-abundance associations, with the highest sampling consensus in CCRCC. Together, these results highlight STAD, KIRC, and CCRCC as cancer lineages where COP1P1 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 COP1P1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes COP1P1 survival associations across molecular data types. COP1P1 RNA expression shows survival associations in the most cancer types (15). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible COP1P1 RNA expression–survival associations across cancer types. High COP1P1 expression shows unfavorable associations in STAD, SKCM, OV and LIHC, but favorable associations in KIRP and KIRC. The STAD 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 STAD as the clearest survival context for COP1P1 RNA expression.
This table summarizes COP1P1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 6. The strongest signals are observed in KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for COP1P1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. COP1P1 shows lower tumor expression in LUAD and higher tumor expression in KIRC, COAD, LIHC, CHOL and BLCA. The KIRC box plot shows higher COP1P1 RNA expression in tumor versus normal tissue (log2 FC = +0.027, t-test p < 0.001).
This table shows molecular features associated with COP1P1 in patient tissues and cancer cell lines. In patient samples, COP1P1 shows the broadest associations at the RNA and protein expression levels, with CCRCC recurring as the lineage with the largest associated feature set.
