KRT8P18

associated omics data
keratin 8 pseudogene 18Genealiases: []

Q-omics provides the consensus-scored KRT8P18 profile across patient tissues and cancer cell-line models. KRT8P18 expression is associated with patient survival in 17 of 34 cancer types, with the highest sampling consensus in LUAD. Among the 18 cancer types available for tumor–normal comparison, KRT8P18 is differentially expressed in 5, with the highest sampling consensus in BRCA. Additionally, KRT8P18 RNA expression shows 9,118 significant gene co-expression associations, with the highest sampling consensus in TGCT. Together, these results highlight LUAD, BRCA, and TGCT as cancer lineages where KRT8P18 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.

Survival associations

This table summarizes KRT8P18 survival associations across molecular data types. KRT8P18 RNA expression shows survival associations in the most cancer types (17). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
KRT8P18 data typeSurvival analysisLineage consensusLineage of highest sampling consensus
RNAKaplan–Meier17LUAD (93)view →
This table ranks reproducible KRT8P18 RNA expression–survival associations across cancer types. High KRT8P18 expression shows unfavorable associations in LUAD, OV, DLBC, PAAD and STAD, but favorable associations in READ. The LUAD 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 LUAD as the clearest survival context for KRT8P18 RNA expression.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
LUADOSMedianAll0.2440.441<.00193view →
OVOSMedianAll0.7990.877.00156view →
READDFSTertileAll0.7630.381.00143view →
DLBCOSTertileIII,IV0.1750.874.02536view →
PAADOSTertileAll0.4830.744.00331view →
STADDFSMedianAll0.6250.781.03024view →
Pink = unfavorable, green = favorable. all 17 lineages →

KRT8P18-LUAD (OS)

Kaplan–Meier survival curve for KRT8P18 RNA expression in LUAD: high vs low expression groups.

Explore this curve interactively →

Tumor vs Normal expression

This table summarizes KRT8P18 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 5. The strongest signals are observed in BRCA for RNA.
KRT8P18 data typeExpression analysisLineage consensusLineage of highest sampling consensus
RNABox plot5BRCA (6)view →
This table ranks reproducible tumor–normal expression differences for KRT8P18. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. KRT8P18 shows lower tumor expression in KIRC and higher tumor expression in BRCA, KIRP, CHOL and PRAD. The BRCA box plot shows higher KRT8P18 RNA expression in tumor versus normal tissue (log2 FC = +0.071, t-test p < 0.001).
LineageGenderStageFold-changepSampling consensus
BRCAAllAll+0.071<.0016view →
KIRPFemaleAll+0.098.0052view →
CHOLAllAll+0.055.0192view →
PRADAllAll+0.034.0082view →
KIRCAllIII,IV−0.022.0232view →
Green = repressed in tumor. all 5 lineages →

KRT8P18-BRCA

Tumor-vs-normal expression box plot for KRT8P18 in BRCA.

Explore this plot interactively →

Cross-omics associations

This table shows molecular features associated with KRT8P18 in patient tissues and cancer cell lines. In patient samples, KRT8P18 shows the broadest associations at the RNA and protein expression levels, with TGCT recurring as the lineage with the largest associated feature set.
Associated data typeStrength (# associated data)Lineage of highest associated data
RNA
RNA9,118TGCT (3481)view →
Function (RNA)6,746UCEC (4341)view →