Homo sapiens Protein: DEK
Summary
InnateDB Protein IDBP-64040.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DEK
Protein Name DEK oncogene
Synonyms D6S231E;
Species Homo sapiens
Ensembl Protein ENSP00000244776
InnateDB Gene IDBG-64038 (DEK)
Protein Structure
UniProt Annotation
Function Involved in chromatin organization. {ECO:0000269PubMed:17524367}.
Subcellular Localization Nucleus {ECO:0000269PubMed:17524367, ECO:0000269PubMed:19695025}. Note=Enriched in regions where chromatin is decondensed or sparse in the interphase nuclei.
Disease Associations Note=A chromosomal aberration involving DEK is found in a subset of acute myeloid leukemia (AML); also known as acute non- lymphocytic leukemia. Translocation t(6;9)(p23;q34) with NUP214/CAN. It results in the formation of a DEK-CAN fusion gene.
Tissue Specificity Ubiquitous. Expressed at relatively high levels.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 43 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 43 [view]
Protein-Protein 43 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0042393 histone binding
GO:0044822 poly(A) RNA binding
Biological Process
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0006366 transcription from RNA polymerase II promoter
GO:0007165 signal transduction
GO:0016568 chromatin modification
GO:0019079 viral genome replication
GO:2000779 regulation of double-strand break repair
Cellular Component
GO:0005634 nucleus
Protein Structure and Domains
PDB ID
InterPro IPR003034 SAP domain
IPR014876 DEK, C-terminal
PFAM PF02037
PF08766
PRINTS
PIRSF
SMART SM00513
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P35659
PhosphoSite PhosphoSite-P35659
TrEMBL
UniProt Splice Variant
Entrez Gene 7913
UniGene Hs.718522
RefSeq NP_001128181
HUGO HGNC:2768
OMIM 125264
CCDS CCDS47382
HPRD 00503
IMGT
EMBL AK297749 AK312616 AL031774 BC035259 CH471087 X64229
GenPept AAH35259 BAG35503 BAG60099 CAA45536 CAI20082 EAW55402