KMT2A / MLLT1 t(11;19) Fusion probe hybridized to patient material showing t(11;19) translocation (2RG1R1G).

RUO - KMT2A / MLLT1

ruo-kmt2a-mllt1

One of the relatively frequently observed translocations (around 10 %) in AML and ALL involves the genes KMT2A (previously known as MLL) and MLLT1 (aka ENL) at 11q23 and 19p13. The KMT2A / MLLT1 translocation results in the generation of fusion protein that retains the MLL N-terminus, including both an A-T hook domain and a region similar to mammalian DNA methyltransferase. There are several breakpoints within the MLLT1 gene described, without clear differences in clinicohematologic features. The KMT2A / MLLT1 Fusion probe is optimized to detect translocations involving the KMT2A and MLLT1 gene regions at 11q23 and 19p13 in a dual-color, fusion assay on metaphase/interphase spreads, blood smears and bone marrow cells in a dual-color, fusion assay.

References:

Mitterbauer-Hohdanner G et al, 2004, Eur J Clin Invest, 34; 12-24.

Meyer C et al, 2009, Leukemia, 23; 1490-1499.

Fu JF et al, 2007, Am J Clin Pathol, 127; 24-30.

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KI-10307
KMT2A/MLLT1 t(11;19) Fusion
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