Q-omics provides the consensus-scored LSP1P1 profile across patient tissues and cancer cell-line models. LSP1P1 expression is associated with patient survival in 15 of 34 cancer types, with the highest sampling consensus in KICH. Among the 18 cancer types available for tumor–normal comparison, LSP1P1 is differentially expressed in 2, with the highest sampling consensus in KIRC. Additionally, LSP1P1 RNA expression shows 6,061 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight KICH, KIRC, and STAD as cancer lineages where LSP1P1 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 LSP1P1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LSP1P1 survival associations across molecular data types. LSP1P1 RNA expression shows survival associations in the most cancer types (15). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LSP1P1 RNA expression–survival associations across cancer types. High LSP1P1 expression shows unfavorable associations in KICH, OV, THYM, LAML and COAD, but favorable associations in MESO. 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 LSP1P1 RNA expression.
This table summarizes LSP1P1 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 KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for LSP1P1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LSP1P1 shows higher tumor expression in KIRC and LUAD. The KIRC box plot shows higher LSP1P1 RNA expression in tumor versus normal tissue (log2 FC = +0.177, t-test p < 0.001).
This table shows molecular features associated with LSP1P1 in patient tissues and cancer cell lines. In patient samples, LSP1P1 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
