Across TCGA cell cohorts, SLC52A2 mutation is significantly associated with the RNA expression of many other genes, with 10 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible SLC52A2-associated genes across cancer lineages are SSMEM1, FAM205A, and MYL7. Each is linked with SLC52A2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC52A2-to-partner and partner-to-SLC52A2 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC52A2→partner) and Y-score (partner→SLC52A2) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.

Lineage	Partner gene	X-score	Y-score	p(X)	p(Y)	Sampling consensus	Lineage consensus
LARGE_INTESTINE	SSMEM1 →	+0.027	+4.029	<.001	.002	3	1
LARGE_INTESTINE	FAM205A →	+0.028	+3.614	<.001	.006	3	1
BLOOD_Leukemia	MYL7 →	+0.105	+4.339	<.001	.002	3	1
BLOOD_Leukemia	HHLA1 →	+0.009	+3.551	<.001	.009	3	1
BLOOD_Leukemia	SLC6A17 →	+0.207	+4.037	<.001	.004	3	1
BLOOD_Leukemia	KHDC3L →	+0.259	+3.774	<.001	.008	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 10 associations by consensus.

Exploration

SLC52A2 survival (RNA) · tumor vs normal (RNA) · all SLC52A2 data types