MIR6835

associated omics data
Gene

Q-omics provides the consensus-scored MIR6835 profile across patient tissues and cancer cell-line models. MIR6835 expression is associated with patient survival in 27 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, MIR6835 is differentially expressed in 9, with the highest sampling consensus in COAD. Additionally, MIR6835 RNA expression shows 16,390 significant gene co-expression associations, with the highest sampling consensus in DLBC. Together, these results highlight KIRC, COAD, and DLBC as cancer lineages where MIR6835 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 MIR6835 survival associations across molecular data types. MIR6835 RNA expression shows survival associations in the most cancer types (27). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
MIR6835 data typeSurvival analysisLineage consensusLineage of highest sampling consensus
RNAKaplan–Meier27KIRC (139)view →
This table ranks reproducible MIR6835 RNA expression–survival associations across cancer types. High MIR6835 expression shows unfavorable associations in KIRC, KIRP, COAD and UVM, but favorable associations in OV and HNSC. 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 MIR6835 RNA expression.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
KIRCDFSMedianIII,IV0.3330.542<.001139view →
KIRPOSMedianII,III,IV0.2610.721<.00197view →
COADOSTertileAll0.7240.870<.00178view →
UVMDFSQuartileAll0.2331.000<.00163view →
OVOSTertileIV0.8040.506<.00156view →
HNSCDFSMedianAll0.7450.647.00447view →
Pink = unfavorable, green = favorable. all 27 lineages →

MIR6835-KIRC (DFS)

Kaplan–Meier survival curve for MIR6835 RNA expression in KIRC: high vs low expression groups.

Explore this curve interactively →

Tumor vs Normal expression

This table summarizes MIR6835 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 9. The strongest signals are observed in COAD for RNA.
MIR6835 data typeExpression analysisLineage consensusLineage of highest sampling consensus
RNABox plot9COAD (10)view →
This table ranks reproducible tumor–normal expression differences for MIR6835. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. MIR6835 shows higher tumor expression in COAD, LUAD, LUSC, STAD, BRCA and LIHC. The COAD box plot shows higher MIR6835 RNA expression in tumor versus normal tissue (log2 FC = +1.534, t-test p < 0.001).
LineageGenderStageFold-changepSampling consensus
COADMaleII,III,IV+1.534<.00110view →
LUADMaleAll+0.978<.0017view →
LUSCAllII,III,IV+1.406<.0016view →
STADAllAll+0.802.0046view →
BRCAAllAll+0.692<.0016view →
LIHCAllAll+0.320<.0015view →
Green = repressed in tumor. all 9 lineages →

MIR6835-COAD

Tumor-vs-normal expression box plot for MIR6835 in COAD.

Explore this plot interactively →

Cross-omics associations

This table shows molecular features associated with MIR6835 in patient tissues and cancer cell lines. In patient samples, MIR6835 shows the broadest associations at the RNA and protein expression levels, with DLBC recurring as the lineage with the largest associated feature set.
Associated data typeStrength (# associated data)Lineage of highest associated data
RNA
RNA16,390DLBC (6613)view →
Protein (mass-spec)8,275LSCC (2651)view →