RSPH6A

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, RSPH6A Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated RSPH6A data layer compared with 19 for mass-spec protein.

The strongest signal is observed in liver hepatocellular carcinoma (LIHC), where higher RSPH6A Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RSPH6A expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

LIHC, PRAD, and LUSC are the cancer types where RSPH6A 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
LIHCDFSMedianAll0.0440.553<.00112view →
PRADDFSMedianAll0.6170.886.0156view →
LUSCDFSMedianAll0.3260.719.0124view →
COADDFSMedianAll0.1330.567.0114view →
UCECOSMedianAll1.0000.654.0302view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

RSPH6A–LIHC (DFS)

Kaplan–Meier survival curve for RSPH6A mutant vs wild-type samples in LIHC.

Open the LIHC breakdown →

Exploration