Q-omics provides the consensus-scored H3P24 profile across patient tissues and cancer cell-line models. H3P24 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in KICH. Among the 18 cancer types available for tumor–normal comparison, H3P24 is differentially expressed in 9, with the highest sampling consensus in UCEC. Additionally, H3P24 RNA expression shows 7,181 significant gene co-expression associations, with the highest sampling consensus in READ. Together, these results highlight KICH, UCEC, and READ as cancer lineages where H3P24 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 H3P24 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes H3P24 survival associations across molecular data types. H3P24 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 H3P24 RNA expression–survival associations across cancer types. High H3P24 expression shows unfavorable associations in KICH, STAD, MESO and LUAD, but favorable associations in UCEC and ACC. The KICH 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 KICH as the clearest survival context for H3P24 RNA expression.
This table summarizes H3P24 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 9. The strongest signals are observed in UCEC for RNA.
This table ranks reproducible tumor–normal expression differences for H3P24. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. H3P24 shows lower tumor expression in KICH and higher tumor expression in UCEC, COAD, KIRP, LUSC and BRCA. The UCEC box plot shows higher H3P24 RNA expression in tumor versus normal tissue (log2 FC = +0.567, t-test p = .007).
This table shows molecular features associated with H3P24 in patient tissues and cancer cell lines. In patient samples, H3P24 shows the broadest associations at the RNA and protein expression levels, with READ recurring as the lineage with the largest associated feature set.
