Q-omics provides the consensus-scored ARF4P1 profile across patient tissues and cancer cell-line models. ARF4P1 expression is associated with patient survival in 22 of 34 cancer types, with the highest sampling consensus in CHOL. Among the 18 cancer types available for tumor–normal comparison, ARF4P1 is differentially expressed in 11, with the highest sampling consensus in COAD. Additionally, ARF4P1 RNA expression shows 9,364 significant gene co-expression associations, with the highest sampling consensus in ACC. Together, these results highlight CHOL, COAD, and ACC as cancer lineages where ARF4P1 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 ARF4P1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes ARF4P1 survival associations across molecular data types. ARF4P1 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 ARF4P1 RNA expression–survival associations across cancer types. High ARF4P1 expression shows unfavorable associations in CHOL, KICH, PAAD and ACC, but favorable associations in THYM and SKCM. The CHOL 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 CHOL as the clearest survival context for ARF4P1 RNA expression.
This table summarizes ARF4P1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 11. The strongest signals are observed in COAD for RNA.
This table ranks reproducible tumor–normal expression differences for ARF4P1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. ARF4P1 shows lower tumor expression in THCA and higher tumor expression in COAD, UCEC, LUAD, BRCA and LIHC. The COAD box plot shows higher ARF4P1 RNA expression in tumor versus normal tissue (log2 FC = +0.721, t-test p < 0.001).
This table shows molecular features associated with ARF4P1 in patient tissues and cancer cell lines. In patient samples, ARF4P1 shows the broadest associations at the RNA and protein expression levels, with ACC recurring as the lineage with the largest associated feature set.
