HAPLN1

Across TCGA pan-cancer cohorts, HAPLN1 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated HAPLN1 data layer compared with 28 for mass-spec protein and 4 for mass-spec protein.

The strongest signal is observed in breast invasive carcinoma (BRCA), where higher HAPLN1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated HAPLN1 expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.

BRCA, LUAD, and COAD are the cancer types where HAPLN1 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
BRCA	OS	Median	All	0.001	0.963	<.001	36	view →
LUAD	OS	Median	III,IV	0.057	0.680	<.001	12	view →
COAD	OS	Median	III,IV	0.056	0.793	<.001	12	view →
UCEC	DFS	Median	All	0.961	0.627	.021	12	view →
SKCM	OS	Median	All	1.000	0.867	.036	2	view →

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

HAPLN1–BRCA (OS)

Open the BRCA breakdown →