Q-omics provides the consensus-scored KRTAP23-1 profile across patient tissues and cancer cell-line models. KRTAP23-1 expression is associated with patient survival in 11 of 34 cancer types, with the highest sampling consensus in BLCA. Additionally, KRTAP23-1 RNA expression shows 6,070 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight BLCA, and STAD as cancer lineages where KRTAP23-1 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 KRTAP23-1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes KRTAP23-1 survival associations across molecular data types. KRTAP23-1 RNA expression shows survival associations in the most cancer types (11). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible KRTAP23-1 RNA expression–survival associations across cancer types. High KRTAP23-1 expression shows unfavorable associations in BLCA, LIHC, CESC, THCA, DLBC and STAD. The BLCA 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 BLCA as the clearest survival context for KRTAP23-1 RNA expression.
This table shows molecular features associated with KRTAP23-1 in patient tissues and cancer cell lines. In patient samples, KRTAP23-1 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set. In cancer cell lines, KRTAP23-1 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in BLOOD_Leukemia, while CRISPR and shRNA rows add functional-dependency signals in LARGE_INTESTINE and CNS.
