Q-omics provides the consensus-scored TRIM31-AS1 profile across patient tissues and cancer cell-line models. TRIM31-AS1 expression is associated with patient survival in 22 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, TRIM31-AS1 is differentially expressed in 13, with the highest sampling consensus in COAD. Additionally, TRIM31-AS1 RNA expression shows 14,732 significant gene co-expression associations, with the highest sampling consensus in THYM. Together, these results highlight ACC, COAD, and THYM as cancer lineages where TRIM31-AS1 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 TRIM31-AS1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes TRIM31-AS1 survival associations across molecular data types. TRIM31-AS1 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 TRIM31-AS1 RNA expression–survival associations across cancer types. High TRIM31-AS1 expression shows unfavorable associations in COAD, but favorable associations in ACC, READ, KIRC, PRAD and CHOL. The ACC Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p < 0.001). Together, the overview and detailed table identify ACC as the clearest survival context for TRIM31-AS1 RNA expression.
This table summarizes TRIM31-AS1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 13. The strongest signals are observed in COAD for RNA.
This table ranks reproducible tumor–normal expression differences for TRIM31-AS1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. TRIM31-AS1 shows lower tumor expression in KICH and BRCA and higher tumor expression in COAD, LUAD, STAD and THCA. The COAD box plot shows higher TRIM31-AS1 RNA expression in tumor versus normal tissue (log2 FC = +1.082, t-test p < 0.001).
This table shows molecular features associated with TRIM31-AS1 in patient tissues and cancer cell lines. In patient samples, TRIM31-AS1 shows the broadest associations at the RNA and protein expression levels, with THYM recurring as the lineage with the largest associated feature set.
