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DEK

Function

Involved in chromatin organization.

Involvement in disease

A chromosomal aberration involving DEK is found in a subset of acute myeloid leukemia (AML); also known as acute non-lymphocytic leukemia (PubMed:1549122). Translocation t(6;9)(p23;q34) with NUP214/CAN (PubMed:1549122). It results in the formation of a DEK-NUP214 fusion gene (PubMed:1549122).

Post-translational modifications

Phosphorylated by CK2. Phosphorylation fluctuates during the cell cycle with a moderate peak during G(1) phase, and weakens the binding of DEK to DNA.

Tissue Specificity

Ubiquitous. Expressed at relatively high levels.

Cellular localization

Alternative names

Protein DEK, DEK

swissprot:P35659 entrezGene:7913 omim:125264