TMEM38A

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, TMEM38A Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated TMEM38A data layer compared with 20 for mass-spec protein and 2 for mass-spec protein.

The strongest signal is observed in colon adenocarcinoma (COAD), where higher TMEM38A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated TMEM38A expression acts as an unfavorable survival marker.

COAD, LUSC, and LIHC are the cancer types where TMEM38A Mutation most reproducibly stratifies survival.

Mutation survival associations by lineage

Ranked by sampling consensus. AUC1 and AUC2 indicate survival in the high- and low-expression groups, respectively; the lower AUC marks the poorer-surviving group. p-values are from the log-rank test.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
COADOSMedianAll0.1680.806.00224view →
LUSCDFSMedianIII,IV0.2350.638.0249view →
LIHCOSMedianAll0.1440.688.0139view →
SKCMDFSMedianAll0.2280.643.0059view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

TMEM38A–COAD (OS)

Kaplan–Meier survival curve for TMEM38A mutant vs wild-type samples in COAD.

Open the COAD breakdown →

Exploration