Q-omics provides the consensus-scored PPP1R12B profile across patient tissues and cancer cell-line models. PPP1R12B expression is associated with patient survival in 30 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, PPP1R12B is differentially expressed in 17, with the highest sampling consensus in THCA. Additionally, PPP1R12B protein abundance shows 35,011 significant protein co-abundance associations, with the highest sampling consensus in GBM. Together, these results highlight KIRC, THCA, and GBM as cancer lineages where PPP1R12B 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 PPP1R12B — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes PPP1R12B survival associations across molecular data types. PPP1R12B RNA expression shows survival associations in the most cancer types (30), followed by mutation status (5) and mass-spec protein abundance (6). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible PPP1R12B RNA expression–survival associations across cancer types. High PPP1R12B expression shows unfavorable associations in ACC, UVM and KIRP, but favorable associations in KIRC, HNSC and UCS. 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 PPP1R12B RNA expression.
This table summarizes PPP1R12B tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 17, while mass-spec protein shows differences in 6. The strongest signals are observed in THCA for RNA and COAD for protein.
This table ranks reproducible tumor–normal expression differences for PPP1R12B. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. PPP1R12B shows lower tumor expression in THCA, BLCA, COAD, LUAD, HNSC and KIRP. The THCA box plot shows higher PPP1R12B RNA expression in normal versus tumor tissue (log2 FC = −1.342, t-test p < 0.001).
This table shows molecular features associated with PPP1R12B in patient tissues and cancer cell lines. In patient samples, PPP1R12B shows the broadest associations at the RNA and protein expression levels, with GBM recurring as the lineage with the largest associated feature set. In cancer cell lines, PPP1R12B RNA and mutation anchors are most strongly linked to RNA-expression features, especially in LIVER, while CRISPR and shRNA rows add functional-dependency signals in OVARY and BLOOD_Leukemia.
