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 
- Species
- Homo sapiens [tax_id: 9606] 
- Genome
- hg38 
ReMap Statistics
- Datasets
- 2
- Biotypes
- 1
- Peaks
- 16,572
- Non-redundant peaks
- 13,389
TF Classification
- Super Class
- NA
- Class
- NA
- Familly
- NA
- Sub Familly
- NA
 Source TFClass
Datasets Table for TBX3
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks | 
|---|---|---|---|---|---|---|---|---|
| TBX3 | Hep-G2 | ENCODE | Homo sapiens | ENCSR238QRG | 12,392 | |||
| TBX3 | Hep-G2 | ENCODE | Homo sapiens | ENCSR605YWG | 4,180 | |||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |