Q-omics provides the consensus-scored KCNIP4-IT1 profile across patient tissues and cancer cell-line models. KCNIP4-IT1 expression is associated with patient survival in 14 of 34 cancer types, with the highest sampling consensus in KIRP. Among the 18 cancer types available for tumor–normal comparison, KCNIP4-IT1 is differentially expressed in 2, with the highest sampling consensus in LUSC. Additionally, KCNIP4-IT1 RNA expression shows 13,375 significant protein co-abundance associations, with the highest sampling consensus in LSCC. Together, these results highlight KIRP, LUSC, and LSCC as cancer lineages where KCNIP4-IT1 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 KCNIP4-IT1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes KCNIP4-IT1 survival associations across molecular data types. KCNIP4-IT1 RNA expression shows survival associations in the most cancer types (14). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible KCNIP4-IT1 RNA expression–survival associations across cancer types. High KCNIP4-IT1 expression shows unfavorable associations in KIRP, HNSC, LIHC, THYM and CHOL, but favorable associations in LAML. The KIRP Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .003). Together, the overview and detailed table identify KIRP as the clearest survival context for KCNIP4-IT1 RNA expression.
This table summarizes KCNIP4-IT1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 2. The strongest signals are observed in LUSC for RNA.
This table ranks reproducible tumor–normal expression differences for KCNIP4-IT1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. KCNIP4-IT1 shows higher tumor expression in LUSC and HNSC. The LUSC box plot shows higher KCNIP4-IT1 RNA expression in tumor versus normal tissue (log2 FC = +0.011, t-test p = .003).
This table shows molecular features associated with KCNIP4-IT1 in patient tissues and cancer cell lines. In patient samples, KCNIP4-IT1 shows the broadest associations at the RNA and protein expression levels, with LSCC recurring as the lineage with the largest associated feature set.
