SPPL2C

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, SPPL2C Mutation is linked to patient survival in 9 of 34 cancer types, making it a survival-associated SPPL2C data layer compared with 16 for mass-spec protein.

The strongest signal is observed in esophageal carcinoma (ESCA), where higher SPPL2C Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SPPL2C expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

ESCA, LUSC, and CHOL are the cancer types where SPPL2C 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
ESCAOSMedianAll0.1980.872.00318view →
LUSCOSMedianIV0.0010.673.01412view →
CHOLOSMedianAll0.0890.727.0019view →
PRADDFSMedianAll0.0850.774<.0016view →
UCECDFSMedianII,III,IV1.0000.442.0286view →
LUADOSMedianII,III,IV0.0790.683<.0016view →
LGGDFSMedianAll0.1850.826<.0013view →
SARCDFSMedianAll0.1640.517.0353view →
HNSCDFSMedianIV0.1480.669.0203view →
Pink = unfavorable, green = favorable. Showing the 9 strongest of 9 lineages.

Exploration