Q-omics provides the consensus-scored HNRNPA1P12 profile across patient tissues and cancer cell-line models. HNRNPA1P12 expression is associated with patient survival in 22 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, HNRNPA1P12 is differentially expressed in 8, with the highest sampling consensus in COAD. Additionally, HNRNPA1P12 RNA expression shows 16,170 significant gene co-expression associations, with the highest sampling consensus in ACC. Together, these results highlight KIRC, COAD, and ACC as cancer lineages where HNRNPA1P12 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 HNRNPA1P12 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes HNRNPA1P12 survival associations across molecular data types. HNRNPA1P12 RNA expression shows survival associations in the most cancer types (22), followed by mutation status (1). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible HNRNPA1P12 RNA expression–survival associations across cancer types. High HNRNPA1P12 expression shows unfavorable associations in ACC and LIHC, but favorable associations in KIRC, CESC, BRCA and THCA. 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 HNRNPA1P12 RNA expression.
This table summarizes HNRNPA1P12 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 8. The strongest signals are observed in COAD for RNA.
This table ranks reproducible tumor–normal expression differences for HNRNPA1P12. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. HNRNPA1P12 shows higher tumor expression in COAD, HNSC, LIHC, CHOL, KIRC and LUSC. The COAD box plot shows higher HNRNPA1P12 RNA expression in tumor versus normal tissue (log2 FC = +0.370, t-test p < 0.001).
This table shows molecular features associated with HNRNPA1P12 in patient tissues and cancer cell lines. In patient samples, HNRNPA1P12 shows the broadest associations at the RNA and protein expression levels, with ACC recurring as the lineage with the largest associated feature set.
