Homo sapiens Gene: TLX2
Summary
InnateDB Gene IDBG-57593.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TLX2
Gene Name T-cell leukemia homeobox 2
Synonyms HOX11L1; NCX
Species Homo sapiens
Ensembl Gene ENSG00000115297
Encoded Proteins
T-cell leukemia homeobox 2
T-cell leukemia homeobox 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene is a member of an orphan homeobox-containing transcription factor family. Studies of the mouse ortholog have shown that the encoded protein is crucial for the development of the enteric nervous system; in humans, loss-of-function may play a role in tumorigenesis of gastrointestinal stromal tumors. [provided by RefSeq, May 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:74513463-74517147
Strand Forward strand
Band p13.1
Transcripts
ENST00000233638 ENSP00000233638
ENST00000497238
ENST00000464417
ENST00000621092 ENSP00000482690
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 10 experimentally validated interaction(s) in this database.
Experimentally validated
Total 10 [view]
Protein-Protein 10 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
GO:0003677 DNA binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0005515 protein binding
GO:0043565 sequence-specific DNA binding
Biological Process
GO:0001707 mesoderm formation
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0008150 biological_process
GO:0048484 enteric nervous system development
GO:0050774 negative regulation of dendrite morphogenesis
Cellular Component
GO:0005575 cellular_component
GO:0005634 nucleus
GO:0005737 cytoplasm
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
KEGG
INOH
PID NCI
ALK2 signaling events
ALK1 signaling events
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.168586
RefSeq NM_016170
HUGO
OMIM
CCDS CCDS1947
HPRD 07254
IMGT
EMBL
GenPept
RNA Seq Atlas