Table 5. Suppression of PEV and TPE by Chromodomain Proteins.

Gene	Allele	Type of Mutation	PEV	TPE
Su(var)3-9	Su(var)3-9330	Point mutation	+++	+++
HP1a	Su(var)2-54	Point mutation	+++	−
	Su(var)2-55	Point mutation	+++	−
	Df(2L)28E4-7;29B2-C1	Deficiency	++	−
CG8120 a	Df(3R)85D8-12; 85E7-F1	Deficiency	−	+
	Df(3R)85D10-12; 85E1-3	Deficiency	−	+
HP1c a	Df(3R)93E-F; 94C-D	Deficiency	−	++
CG15636 a	Df(2L)24C2-8;025C8-9	Deficiency	++	−
Chro	Df(3L)79E2+;80; 70D1-2	Deficiency	+++	−
msl-3	msl-31	Point mutation	−	+
MRG15	Df(3R)88E7-13; 89A1	Deficiency	−	+
kis	kis1	Point mutation	−	+
	Df(2L)21A1; 21B6-7PMC	Deficiency	−	++
	Df(2L)21A1; 21B6-7PM47C	Deficiency	−	++
Chd1	Df(2L)23C1-2; 23E1-2	Deficiency	+	−
Mi-2	Df(3L)76B; 77A b	Deficiency	++	+
CHD3	Df(3L)76B; 77A b	Deficiency	++	+
Pc	Pc1	Point mutation	−	−

^a CG8120, HP1c, and CG15636 also have chromo shadow domains and are putative paralogs of HP1a.

^balso removes Kap-α1 (see Table 7).