Q-omics provides the consensus-scored C1DP3 profile across patient tissues and cancer cell-line models. C1DP3 expression is associated with patient survival in 12 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, C1DP3 is differentially expressed in 1, with the highest sampling consensus in LUAD. Additionally, C1DP3 RNA expression shows 5,870 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight KIRC, LUAD, and STAD as cancer lineages where C1DP3 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 C1DP3 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes C1DP3 survival associations across molecular data types. C1DP3 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 C1DP3 RNA expression–survival associations across cancer types. High C1DP3 expression shows unfavorable associations in KIRC, BRCA, LIHC, HNSC and ACC, but favorable associations in UCS. The KIRC 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 KIRC as the clearest survival context for C1DP3 RNA expression.
This table summarizes C1DP3 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 C1DP3. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. C1DP3 shows lower tumor expression in LUAD. The LUAD box plot shows higher C1DP3 RNA expression in normal versus tumor tissue (log2 FC = −0.048, t-test p = .009).
This table shows molecular features associated with C1DP3 in patient tissues and cancer cell lines. In patient samples, C1DP3 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
