Q-omics provides the consensus-scored THUMPD3-AS1 profile across patient tissues and cancer cell-line models. THUMPD3-AS1 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in LIHC. Among the 18 cancer types available for tumor–normal comparison, THUMPD3-AS1 is differentially expressed in 11, with the highest sampling consensus in KIRC. Additionally, THUMPD3-AS1 RNA expression shows 20,256 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight LIHC, KIRC, and UVM as cancer lineages where THUMPD3-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 THUMPD3-AS1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes THUMPD3-AS1 survival associations across molecular data types. THUMPD3-AS1 RNA expression shows survival associations in the most cancer types (20). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible THUMPD3-AS1 RNA expression–survival associations across cancer types. High THUMPD3-AS1 expression shows unfavorable associations in LIHC, ACC, KIRC and KICH, but favorable associations in UCS and BLCA. The LIHC 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 LIHC as the clearest survival context for THUMPD3-AS1 RNA expression.
This table summarizes THUMPD3-AS1 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 KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for THUMPD3-AS1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. THUMPD3-AS1 shows lower tumor expression in KIRC and KICH and higher tumor expression in COAD, LIHC, STAD and CHOL. The KIRC box plot shows higher THUMPD3-AS1 RNA expression in normal versus tumor tissue (log2 FC = −0.633, t-test p < 0.001).
This table shows molecular features associated with THUMPD3-AS1 in patient tissues and cancer cell lines. In patient samples, THUMPD3-AS1 shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set.
