NCIt definition : A fusion gene that results from a chromosomal translocation t(15;17)(q22;q21) which
fuses the first 3 exons of the PML gene with the last 7 exons of the RARA gene. This
fusion is associated with acute promyelocytic leukemia. Three transcript variants
are possible based on the three breakpoint clusters in the PML gene.;
NCIt note : The translocation, well known as t(15;17)(q22;q21) or t(15;17)(q22;q12), should be
re-named t(15;17)(q24;q21), since the PML gene is located in the vicinity of 15q24,
and the RARA gene is located in the vicinity of 17q21. (Atlas of Genetics and Cytogenetics
in Oncology and Haematology);