Publication for CHD3 and RAI1

Species	Symbol	Function*	Entrez Gene ID*	Other ID	Gene coexpression	CoexViewer
hsa	CHD3	chromodomain helicase DNA binding protein 3	1107			[link]
hsa	RAI1	retinoic acid induced 1	10743

Pubmed ID	Priority	Text
28055972	0.90	CHD3, RAI1, KMT2A, TCF20, PHF21B, PHF11, EP300, and BRD1.
	0.89	CHD3, RAI1, and PHF11 had more deletions in Luminal, HER2+, or basal-like subtypes, while KMT2A, TCF20, PHF21B, EP300, and BRD1 had more deletions in the Luminal B subtype (Figure 1B, Supplementary Table S4).