RAB33A

Across TCGA pan-cancer cohorts, RAB33A Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RAB33A data layer compared with 25 for mass-spec protein and 1 for mass-spec protein.

The strongest signal is observed in kidney renal papillary cell carcinoma (KIRP), where higher RAB33A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated RAB33A expression acts as an unfavorable survival marker.

KIRP, LIHC, and UCEC are the cancer types where RAB33A 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
KIRP	OS	Median	All	0.199	0.903	<.001	15	view →
LIHC	OS	Median	III,IV	0.270	0.732	.021	12	view →
UCEC	OS	Median	IV	0.231	0.592	.036	6	view →

Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

RAB33A–KIRP (OS)

Open the KIRP breakdown →