MIR3926-1

associated omics data
Gene

Q-omics provides the consensus-scored MIR3926-1 profile across patient tissues and cancer cell-line models. MIR3926-1 expression is associated with patient survival in 15 of 34 cancer types, with the highest sampling consensus in MESO. Among the 18 cancer types available for tumor–normal comparison, MIR3926-1 is differentially expressed in 4, with the highest sampling consensus in BRCA. Additionally, MIR3926-1 RNA expression shows 10,499 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight MESO, BRCA, and UVM as cancer lineages where MIR3926-1 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 MIR3926-1 survival associations across molecular data types. MIR3926-1 RNA expression shows survival associations in the most cancer types (15). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
MIR3926-1 data typeSurvival analysisLineage consensusLineage of highest sampling consensus
RNAKaplan–Meier15MESO (27)view →
This table ranks reproducible MIR3926-1 RNA expression–survival associations across cancer types. High MIR3926-1 expression shows unfavorable associations in MESO, BRCA, ACC and UVM, but favorable associations in LIHC and PRAD. The MESO Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .023). Together, the overview and detailed table identify MESO as the clearest survival context for MIR3926-1 RNA expression.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
MESOOSTertileII,III,IV0.1950.577.02327view →
BRCADFSTertileAll0.8740.910.00524view →
LIHCOSTertileII,III,IV1.0000.415.02924view →
ACCDFSTertileIV0.0570.404.01118view →
PRADDFSTertileAll0.8980.743.01318view →
UVMDFSMedianIII,IV0.3720.685.01718view →
Pink = unfavorable, green = favorable. all 15 lineages →

MIR3926-1-MESO (OS)

Kaplan–Meier survival curve for MIR3926-1 RNA expression in MESO: high vs low expression groups.

Explore this curve interactively →

Tumor vs Normal expression

This table summarizes MIR3926-1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 4. The strongest signals are observed in BRCA for RNA.
MIR3926-1 data typeExpression analysisLineage consensusLineage of highest sampling consensus
RNABox plot4BRCA (8)view →
This table ranks reproducible tumor–normal expression differences for MIR3926-1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. MIR3926-1 shows lower tumor expression in BRCA, LUSC and COAD and higher tumor expression in BLCA. The BRCA box plot shows higher MIR3926-1 RNA expression in normal versus tumor tissue (log2 FC = −0.355, t-test p < 0.001).
LineageGenderStageFold-changepSampling consensus
BRCAFemaleII,III,IV−0.355<.0018view →
LUSCMaleIII,IV−0.972.0102view →
BLCAMaleAll+0.499.0292view →
COADAllII,III,IV−0.150.0311view →
Green = repressed in tumor. all 4 lineages →

MIR3926-1-BRCA

Tumor-vs-normal expression box plot for MIR3926-1 in BRCA.

Explore this plot interactively →

Cross-omics associations

This table shows molecular features associated with MIR3926-1 in patient tissues and cancer cell lines. In patient samples, MIR3926-1 shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set.
Associated data typeStrength (# associated data)Lineage of highest associated data
RNA
RNA10,499UVM (6003)view →
Function (RNA)6,577BRCA (3526)view →