Q-omics provides the consensus-scored RBM39P1 profile across patient tissues and cancer cell-line models. RBM39P1 expression is associated with patient survival in 22 of 34 cancer types, with the highest sampling consensus in CESC. Among the 18 cancer types available for tumor–normal comparison, RBM39P1 is differentially expressed in 7, with the highest sampling consensus in COAD. Additionally, RBM39P1 RNA expression shows 14,168 significant gene co-expression associations, with the highest sampling consensus in ACC. Together, these results highlight CESC, COAD, and ACC as cancer lineages where RBM39P1 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 RBM39P1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RBM39P1 survival associations across molecular data types. RBM39P1 RNA expression shows survival associations in the most cancer types (22). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RBM39P1 RNA expression–survival associations across cancer types. High RBM39P1 expression shows unfavorable associations in ACC, LIHC and STAD, but favorable associations in CESC, SKCM and CHOL. The CESC Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p = .001). Together, the overview and detailed table identify CESC as the clearest survival context for RBM39P1 RNA expression.
This table summarizes RBM39P1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 7. The strongest signals are observed in COAD for RNA.
This table ranks reproducible tumor–normal expression differences for RBM39P1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RBM39P1 shows higher tumor expression in COAD, LIHC, BRCA, HNSC, LUSC and CHOL. The COAD box plot shows higher RBM39P1 RNA expression in tumor versus normal tissue (log2 FC = +0.688, t-test p < 0.001).
This table shows molecular features associated with RBM39P1 in patient tissues and cancer cell lines. In patient samples, RBM39P1 shows the broadest associations at the RNA and protein expression levels, with ACC recurring as the lineage with the largest associated feature set.
