SHISA3

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, SHISA3 Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated SHISA3 data layer compared with 23 for mass-spec protein and 2 for mass-spec protein.

The strongest signal is observed in pheochromocytoma and paraganglioma (PCPG), where higher SHISA3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SHISA3 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.

PCPG, DLBC, and LIHC are the cancer types where SHISA3 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
PCPGOSMedianAll0.0090.946<.00112view →
DLBCOSMedianAll0.0530.936<.00112view →
LIHCDFSMedianAll0.0440.553<.00112view →
PRADDFSMedianAll0.0850.774<.0016view →
UCECOSMedianIV0.2310.592.0366view →
SKCMDFSMedianII,III,IV0.7360.220.0451view →
Pink = unfavorable, green = favorable. Showing the 6 strongest of 6 lineages.

SHISA3–PCPG (OS)

Kaplan–Meier survival curve for SHISA3 mutant vs wild-type samples in PCPG.

Open the PCPG breakdown →

Exploration