Q-omics provides the consensus-scored SUPT4H1P1 profile across patient tissues and cancer cell-line models. SUPT4H1P1 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in UVM. Among the 18 cancer types available for tumor–normal comparison, SUPT4H1P1 is differentially expressed in 7, with the highest sampling consensus in COAD. Additionally, SUPT4H1P1 RNA expression shows 13,700 significant protein co-abundance associations, with the highest sampling consensus in LSCC. Together, these results highlight UVM, COAD, and LSCC as cancer lineages where SUPT4H1P1 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 SUPT4H1P1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes SUPT4H1P1 survival associations across molecular data types. SUPT4H1P1 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 SUPT4H1P1 RNA expression–survival associations across cancer types. High SUPT4H1P1 expression shows unfavorable associations in UVM, ACC and STAD, but favorable associations in BLCA, LUSC and LIHC. The UVM 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 UVM as the clearest survival context for SUPT4H1P1 RNA expression.
This table summarizes SUPT4H1P1 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 SUPT4H1P1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. SUPT4H1P1 shows higher tumor expression in COAD, BLCA, LUSC, BRCA, LUAD and PRAD. The COAD box plot shows higher SUPT4H1P1 RNA expression in tumor versus normal tissue (log2 FC = +0.514, t-test p < 0.001).
This table shows molecular features associated with SUPT4H1P1 in patient tissues and cancer cell lines. In patient samples, SUPT4H1P1 shows the broadest associations at the RNA and protein expression levels, with LSCC recurring as the lineage with the largest associated feature set.
