Homo sapiens Gene: TBX10
Summary
InnateDB Gene IDBG-60905.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TBX10
Gene Name T-box 10
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000167800
Encoded Proteins
T-box 10
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the T-box family of transcription factors. These transcription factors share a DNA-binding domain called the T-box, and play a role in several developmental processes including early embryonic cell fate and organogenesis. The encoded protein is a member of the T-box 1 subfamily. Mutations in this gene are thought to be a cause of isolated cleft lip with or without cleft palate. [provided by RefSeq, Nov 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 11:67631303-67639560
Strand Reverse strand
Band q13.2
Transcripts
ENST00000335385 ENSP00000335191
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0003700 sequence-specific DNA binding transcription factor activity
Biological Process
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0009653 anatomical structure morphogenesis
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt O75333
TrEMBL
UniProt Splice Variant
Entrez Gene 347853
UniGene Hs.454480
RefSeq NM_005995
HUGO HGNC:11593
OMIM 604648
CCDS CCDS31621
HPRD
IMGT
EMBL AH006177 AY229977 BC113485 BC113487
GenPept AAC23481 AAI13486 AAI13488 AAO73483
RNA Seq Atlas 347853