TBX3
Information TBX3
- Description
This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This protein is a transcriptional repressor and is thought to play a role in the anterior/posterior axis of the tetrapod forelimb. Mutations in this gene cause ulnar-mammary syndrome, affecting limb, apocrine gland, tooth, hair, and genital development. Alternative splicing of this gene results in three transcript variants encoding different isoforms; however, the full length nature of one variant has not been determined. [provided by RefSeq, Jul 2008]
- Full Name
T-box transcription factor 3
- Source NCBI
ReMap Statistics
- Datasets
- 2
- Biotypes
- 1
- Peaks
- 16,575
- Non-redundant peaks
- 13,390
TF Classification
- Super Class
- NA
- Class
- NA
- Familly
- NA
- Sub Familly
- NA
Source TFClass
External IDs
- JASPAR
- Ensembl
- ENSG00000135111
- UniProt
- O15119
- Genevisible
- O15119
- RefSeq
- NM_005996
- Aliases
- TBX3-ISO; UMS; XHL
Datasets Table for TBX3
Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |
---|---|---|---|---|---|---|---|---|
TBX3 | Hep-G2 | ENCODE | Homo sapiens | ENCSR238QRG | 12,395 | |||
TBX3 | Hep-G2 | ENCODE | Homo sapiens | ENCSR605YWG | 4,180 | |||
Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |