Table 4.

Reported cytogenetic abnormalities involving Xp11.2 translocation RCC

Cytogenetic translocations involving Xp11.2 translocation RCC				Other genetic abnormalities
Chromosome Translocation	Gene Fusion	Neoplasm	Source, year	Chromosome or gene aberrations	Source, year
t(X;1)(p11.2;q21)	PRCC-TFE3	RCC	Argani et al, 16 2007	t(X;1)(p11.2;p34) coexistent VHL gene mutation	Parast et al, 2004
t(X;1)(p11.2;p34)	PSF-TFE3	RCC	Argani et al, 16 2007
t(X;17)(p11.2;q25)	ASPL-TFE3	RCC	Argani et al, 16 2007
inv(X)(p11.2;q12)	NONO-TFE3	RCC	Argani et al, 16 2007	chromosome 7, 8, 12, 17 trisomy, +add(X), loss of the Y	Altinok et al, 2005
t(X;17)(p11.2;q23)	CLTC-TFE3	RCC	Argani et al, 8 2003
t(X;3)(p11.2;q23)	Unknown	RCC	Argani et al, 16 2007
t(X;10)(p11.2;q23)	Unknown	RCC	Dijkuizen et al, 1995	deletion of 3p25-26	Bruder et al, 2004
t((X;19)(p11.2;q13.1)	Unknown	RCC	Armah et al, 2009