Q-omics provides the consensus-scored SPINT1-AS1 profile across patient tissues and cancer cell-line models. SPINT1-AS1 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, SPINT1-AS1 is differentially expressed in 11, with the highest sampling consensus in KIRP. Additionally, SPINT1-AS1 RNA expression shows 13,850 significant gene co-expression associations, with the highest sampling consensus in PAAD. Together, these results highlight KIRC, KIRP, and PAAD as cancer lineages where SPINT1-AS1 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 SPINT1-AS1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes SPINT1-AS1 survival associations across molecular data types. SPINT1-AS1 RNA expression shows survival associations in the most cancer types (20). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible SPINT1-AS1 RNA expression–survival associations across cancer types. High SPINT1-AS1 expression shows unfavorable associations in SKCM and ACC, but favorable associations in KIRC, UVM, KIRP and MESO. The KIRC Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p < 0.001). Together, the overview and detailed table identify KIRC as the clearest survival context for SPINT1-AS1 RNA expression.
This table summarizes SPINT1-AS1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 11. The strongest signals are observed in KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for SPINT1-AS1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. SPINT1-AS1 shows lower tumor expression in KIRP and KIRC and higher tumor expression in BLCA, BRCA, CHOL and UCEC. The KIRP box plot shows higher SPINT1-AS1 RNA expression in normal versus tumor tissue (log2 FC = −2.264, t-test p < 0.001).
This table shows molecular features associated with SPINT1-AS1 in patient tissues and cancer cell lines. In patient samples, SPINT1-AS1 shows the broadest associations at the RNA and protein expression levels, with PAAD recurring as the lineage with the largest associated feature set.
