APCDD1L-DT

associated omics data
Gene

Q-omics provides the consensus-scored APCDD1L-DT profile across patient tissues and cancer cell-line models. APCDD1L-DT expression is associated with patient survival in 24 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, APCDD1L-DT is differentially expressed in 12, with the highest sampling consensus in KIRC. Additionally, APCDD1L-DT RNA expression shows 15,911 significant gene co-expression associations, with the highest sampling consensus in THYM. Together, these results highlight KIRC, and THYM as cancer lineages where APCDD1L-DT 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 APCDD1L-DT survival associations across molecular data types. APCDD1L-DT RNA expression shows survival associations in the most cancer types (24). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
APCDD1L-DT data typeSurvival analysisLineage consensusLineage of highest sampling consensus
RNAKaplan–Meier24KIRC (142)view →
This table ranks reproducible APCDD1L-DT RNA expression–survival associations across cancer types. High APCDD1L-DT expression shows unfavorable associations in KIRC, MESO, LUSC, KIRP, STAD and BLCA. The KIRC 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 KIRC as the clearest survival context for APCDD1L-DT RNA expression.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
KIRCDFSQuartileAll0.4950.700<.001142view →
MESOOSTertileAll0.3220.671<.001129view →
LUSCOSMedianAll0.5990.738<.00199view →
KIRPDFSQuartileII,III,IV0.0970.661<.00188view →
STADDFSMedianAll0.3240.627<.00164view →
BLCAOSQuartileAll0.3130.563.00163view →
Pink = unfavorable, green = favorable. all 24 lineages →

APCDD1L-DT-KIRC (DFS)

Kaplan–Meier survival curve for APCDD1L-DT RNA expression in KIRC: high vs low expression groups.

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Tumor vs Normal expression

This table summarizes APCDD1L-DT tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 12. The strongest signals are observed in KIRC for RNA.
APCDD1L-DT data typeExpression analysisLineage consensusLineage of highest sampling consensus
RNABox plot12KIRC (12)view →
This table ranks reproducible tumor–normal expression differences for APCDD1L-DT. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. APCDD1L-DT shows lower tumor expression in KIRC, KIRP and KICH and higher tumor expression in LUSC, LUAD and HNSC. The KIRC box plot shows higher APCDD1L-DT RNA expression in normal versus tumor tissue (log2 FC = −1.669, t-test p < 0.001).
LineageGenderStageFold-changepSampling consensus
KIRCMaleAll−1.669<.00112view →
KIRPMaleAll−2.098<.00111view →
LUSCMaleAll+0.596<.0018view →
LUADAllAll+0.298<.0018view →
KICHFemaleAll−1.747<.0017view →
HNSCFemaleAll+0.871.0027view →
Green = repressed in tumor. all 12 lineages →

APCDD1L-DT-KIRC

Tumor-vs-normal expression box plot for APCDD1L-DT in KIRC.

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Cross-omics associations

This table shows molecular features associated with APCDD1L-DT in patient tissues and cancer cell lines. In patient samples, APCDD1L-DT shows the broadest associations at the RNA and protein expression levels, with THYM recurring as the lineage with the largest associated feature set.
Associated data typeStrength (# associated data)Lineage of highest associated data
RNA
RNA15,911THYM (6573)view →
Protein (mass-spec)9,752COAD (2723)view →