Q-omics provides the consensus-scored KRT8P7 profile across patient tissues and cancer cell-line models. KRT8P7 expression is associated with patient survival in 18 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, KRT8P7 is differentially expressed in 10, with the highest sampling consensus in KIRP. Additionally, KRT8P7 RNA expression shows 8,923 significant gene co-expression associations, with the highest sampling consensus in ESCA. Together, these results highlight ACC, KIRP, and ESCA as cancer lineages where KRT8P7 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 KRT8P7 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes KRT8P7 survival associations across molecular data types. KRT8P7 RNA expression shows survival associations in the most cancer types (18). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible KRT8P7 RNA expression–survival associations across cancer types. High KRT8P7 expression shows unfavorable associations in PAAD, MESO, UCEC and ESCA, but favorable associations in ACC and SKCM. The ACC Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p = .001). Together, the overview and detailed table identify ACC as the clearest survival context for KRT8P7 RNA expression.
This table summarizes KRT8P7 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 10. The strongest signals are observed in KIRP for RNA.
This table ranks reproducible tumor–normal expression differences for KRT8P7. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. KRT8P7 shows higher tumor expression in KIRP, LUAD, BRCA, STAD, LUSC and CHOL. The KIRP box plot shows higher KRT8P7 RNA expression in tumor versus normal tissue (log2 FC = +0.427, t-test p < 0.001).
This table shows molecular features associated with KRT8P7 in patient tissues and cancer cell lines. In patient samples, KRT8P7 shows the broadest associations at the RNA and protein expression levels, with ESCA recurring as the lineage with the largest associated feature set.
