We have shown that the insulin-like growth factor type I and II recept
ors are expressed equally from the maternal and paternal alleles in hu
man tissues. The imprinting status of the type I insulin-like growth f
actor receptor has not been reported while the type II receptor has pr
eviously been shown to be maternally expressed in the mouse. That the
imprinting of the insulin-like growth factor type II receptor is not c
onserved between mouse and humans suggests that the physiological role
of the IGF2 receptor may differ between these two species.