Homo sapiens Gene: TBX15
Summary
InnateDB Gene IDBG-101478.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TBX15
Gene Name T-box 15
Synonyms TBX14
Species Homo sapiens
Ensembl Gene ENSG00000092607
Encoded Proteins
T-box 15
T-box 15
T-box 15
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene belongs to the T-box family of genes, which encode a phylogenetically conserved family of transcription factors that regulate a variety of developmental processes. All these genes contain a common T-box DNA-binding domain. Mutations in this gene are associated with Cousin syndrome.[provided by RefSeq, Oct 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 1:118883046-118989556
Strand Reverse strand
Band p12
Transcripts
ENST00000207157 ENSP00000207157
ENST00000369429 ENSP00000358437
ENST00000449873 ENSP00000398625
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000976 transcription regulatory region sequence-specific DNA binding
GO:0001106 RNA polymerase II transcription corepressor activity
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0042803 protein homodimerization activity
GO:0046982 protein heterodimerization activity
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0048701 embryonic cranial skeleton morphogenesis
GO:0048704 embryonic skeletal system morphogenesis
Cellular Component
GO:0005634 nucleus
GO:0070722 Tle3-Aes complex
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL Q5JT55
UniProt Splice Variant
Entrez Gene 6913
UniGene Hs.146196 Hs.626431
RefSeq XM_005271161 NM_152380 XM_005271162
HUGO HGNC:11594
OMIM 604127
CCDS CCDS30816
HPRD 16035
IMGT
EMBL AL139420 AL357045
GenPept
RNA Seq Atlas 6913