Homo sapiens Protein: MLLT10
Summary
InnateDB Protein IDBP-60819.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MLLT10
Protein Name myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 10
Synonyms AF10;
Species Homo sapiens
Ensembl Protein ENSP00000366272
InnateDB Gene IDBG-60813 (MLLT10)
Protein Structure
UniProt Annotation
Function Probably involved in transcriptional regulation. In vitro or as fusion protein with KMT2A/MLL1 has transactivation activity. Binds to cruciform DNA. {ECO:0000269PubMed:17868029}.
Subcellular Localization Nucleus {ECO:0000269PubMed:10860745}.
Disease Associations Note=A chromosomal aberration involving MLLT10 is associated with acute leukemias. Translocation t(10;11)(p12;q23) with KMT2A/MLL1. The result is a rogue activator protein.Note=A chromosomal aberration involving MLLT10 is associated with diffuse histiocytic lymphomas. Translocation t(10;11)(p13;q14) with PICALM.
Tissue Specificity Expressed abundantly in testis.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 23 experimentally validated interaction(s) in this database.
They are also associated with 7 interaction(s) predicted by orthology.
Experimentally validated
Total 23 [view]
Protein-Protein 22 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 7 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0005515 protein binding
GO:0008270 zinc ion binding
Biological Process
GO:0006351 transcription, DNA-templated
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
Protein Structure and Domains
PDB ID
InterPro IPR001965 Zinc finger, PHD-type
IPR011011 Zinc finger, FYVE/PHD-type
IPR019787 Zinc finger, PHD-finger
PFAM PF00628
PRINTS
PIRSF
SMART SM00249
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P55197
PhosphoSite PhosphoSite-P55197
TrEMBL Q71UR7
UniProt Splice Variant
Entrez Gene 8028
UniGene Hs.605494
RefSeq NP_004632
HUGO HGNC:16063
OMIM 602409
CCDS CCDS7135
HPRD 03874
IMGT
EMBL AF060934 AL161799 AL357372 AL358780 AL359697 AY598745 BC080577 BC094844 BC129946 U13948
GenPept AAA79972 AAC16706 AAH80577 AAT47519 CAH73410 CAI13979 CAI13982 CAI13983 CAI39663 CAI41348