Homo sapiens Protein: TAL2
Summary
InnateDB Protein IDBP-79718.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TAL2
Protein Name T-cell acute lymphocytic leukemia 2
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000334547
InnateDB Gene IDBG-79714 (TAL2)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations Note=A chromosomal aberration involving TAL2 may be a cause of some T-cell acute lymphoblastic leukemia (T-ALL). Translocation t(7;9)(q34;q32) with TCRB.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 7 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
Experimentally validated
Total 7 [view]
Protein-Protein 7 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0046983 protein dimerization activity
Biological Process
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0009791 post-embryonic development
GO:0021794 thalamus development
GO:0030901 midbrain development
GO:0035264 multicellular organism growth
Cellular Component
Protein Structure and Domains
PDB ID
InterPro IPR011598 Myc-type, basic helix-loop-helix (bHLH) domain
PFAM PF00010
PRINTS
PIRSF
SMART SM00353
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q16559
PhosphoSite PhosphoSite-Q16559
TrEMBL
UniProt Splice Variant
Entrez Gene 6887
UniGene Hs.247978
RefSeq NP_005412
HUGO HGNC:11557
OMIM 186855
CCDS CCDS6767
HPRD 01735
IMGT
EMBL AL158070 BC069422 BC126373 BC126375 M81078 S69377
GenPept AAA60613 AAC60629 AAH69422 AAI26374 AAI26376 CAC22163