Homo sapiens Gene: TAL2
Summary
InnateDB Gene IDBG-79714.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TAL2
Gene Name T-cell acute lymphocytic leukemia 2
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000186051
Encoded Proteins
T-cell acute lymphocytic leukemia 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This intronless gene encodes a helix-loop-helix protein. Translocations between this gene on chromosome 9 and the T-cell receptor beta-chain locus on chromosome 7 have been associated with activation of the T-cell acute lymphocytic leukemia 2 gene and T-cell acute lymphoblastic leukemia. [provided by RefSeq, Mar 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 9:105662457-105663112
Strand Forward strand
Band q31.2
Transcripts
ENST00000334077 ENSP00000334547
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
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q16559
TrEMBL
UniProt Splice Variant
Entrez Gene 6887
UniGene Hs.247978
RefSeq NM_005421
HUGO HGNC:11557
OMIM 186855
CCDS CCDS6767
HPRD
IMGT
EMBL AL158070 BC069422 BC126373 BC126375 M81078 S69377
GenPept AAA60613 AAC60629 AAH69422 AAI26374 AAI26376 CAC22163
RNA Seq Atlas 6887