Q-omics provides the consensus-scored KRT18P1 profile across patient tissues and cancer cell-line models. KRT18P1 expression is associated with patient survival in 17 of 34 cancer types, with the highest sampling consensus in BLCA. Among the 18 cancer types available for tumor–normal comparison, KRT18P1 is differentially expressed in 12, with the highest sampling consensus in KIRP. Additionally, KRT18P1 RNA expression shows 9,240 significant gene co-expression associations, with the highest sampling consensus in TGCT. Together, these results highlight BLCA, KIRP, and TGCT as cancer lineages where KRT18P1 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 KRT18P1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes KRT18P1 survival associations across molecular data types. KRT18P1 RNA expression shows survival associations in the most cancer types (17). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible KRT18P1 RNA expression–survival associations across cancer types. High KRT18P1 expression shows unfavorable associations in CHOL and MESO, but favorable associations in BLCA, THCA, BRCA and CESC. The BLCA Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p = .004). Together, the overview and detailed table identify BLCA as the clearest survival context for KRT18P1 RNA expression.
This table summarizes KRT18P1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 12. The strongest signals are observed in HNSC for RNA.
This table ranks reproducible tumor–normal expression differences for KRT18P1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. KRT18P1 shows higher tumor expression in KIRP, HNSC, COAD, BLCA, BRCA and KIRC. The KIRP box plot shows higher KRT18P1 RNA expression in tumor versus normal tissue (log2 FC = +0.153, t-test p < 0.001).
This table shows molecular features associated with KRT18P1 in patient tissues and cancer cell lines. In patient samples, KRT18P1 shows the broadest associations at the RNA and protein expression levels, with TGCT recurring as the lineage with the largest associated feature set.
