AKR1E2

Across TCGA pan-cancer cohorts, AKR1E2 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated AKR1E2 data layer compared with 20 for mass-spec protein.

The strongest signal is observed in head and neck squamous cell carcinoma (HNSC), where higher AKR1E2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated AKR1E2 expression acts as an unfavorable survival marker.

HNSC, SKCM, and READ are the cancer types where AKR1E2 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.

Lineage	Measure	Split	Stage	AUC1 high	AUC2 low	p	Sampling consensus
HNSC	DFS	Median	All	0.122	0.696	<.001	45	view →
SKCM	OS	Median	All	0.179	0.781	<.001	9	view →
READ	DFS	Median	III,IV	0.082	0.746	<.001	6	view →
PRAD	DFS	Median	All	0.085	0.774	<.001	6	view →
UCEC	OS	Median	IV	0.231	0.592	.036	6	view →

Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

AKR1E2–HNSC (DFS)

Open the HNSC breakdown →