| Gene Name | TBXT |
|
| Specie | Homo sapiens | |
| Full Name | T-box transcription factor T | |
| Also known as | SAVA|T|TFT | |
| Coordinate | chr6:166157656-166168655 | |
| Strand | - | |
| Gene summary | The protein encoded by this gene is an embryonic nuclear transcription factor that binds to a specific DNA element, the palindromic T-site. It binds through a region in its N-terminus, called the T-box, and effects transcription of genes required for mesoderm formation and differentiation. The protein is localized to notochord-derived cells. Variation in this gene was associated with susceptibility to neural tube defects and chordoma. A mutation in this gene was found in a family with sacral agenesis with vertebral anomalies. [provided by RefSeq, Sep 2018] |
| Retroname | Coord | Strand | Genomic Region | ENSG | |
|---|---|---|---|---|---|
| TBXTP1 | chr1:183709534-183709911 | - |
Intragenic Intragenic |
ENSG00000270994 | UCSC |
| >NM_001270484.2 |
| AGAAGGGGTTGTTTTGCTTTTGCTTATTTCCGTCCATTTCCCTCTCTGCGCGCGGACCTTCCTTTTCCAGATGGTGAGAGCCGCGGGGACACCCGACGCCGGGGCAGGCTGATCCACGATCCTGGGTGTGCGTAACGCCGCCTGGGGCTCCGTGGGCGAGGGACGTGTGGGGACAGGTGCACCGGAAACTGCCAGACTGGAGAGTTGAGGCATCGGAGGCGCGAGAACAGCACTACTACTGCGGCGAGACGAGCGCGGCGCATCCCAAAGCCCGGCCAAATGCGCTCGTCCCTGGGAGGGGAGGGAGGCGCGCCTGGAGCGGGGACAGGGCGGCGGCCAAGAGCAGGGAAGGTGGATCTCAGGTAGCGAGTCTGGGCTTCGGGGACGGCGGGGAGGGGAGCCGGACGGGAGGATGAGCTCCCCTGGCACCGAGAGCGCGGGAAAGAGCCTGCAGTACCGAGTGGACCACCTGCTGAGCGCCGTGGAGAATGAGCTGCAGGCGGGCAGCGAGAAGGGCGACCCCACAGAGCGCGAACTGCGCGTGGGCCTGGAGGAGAGCGAGCTGTGGCTGCGCTTCAAGGAGCTCACCAATGAGATGATCGTGACCAAGAACGGCAGGAGGATGTTTCCGGTGCTGAAGGTGAACGTGTCTGGCCTGGACCCCAACGCCATGTACTCCTTCCTGCTGGACTTCGTGGCGGCGGACAACCACCGCTGGAAGTACGTGAACGGGGAATGGGTGCCGGGGGGCAAGCCGGAGCCGCAGGCGCCCAGCTGCGTCTACATCCACCCCGACTCGCCCAACTTCGGGGCCCACTGGATGAAGGCTCCCGTCTCCTTCAGCAAAGTCAAGCTCACCAACAAGCTCAACGGAGGGGGCCAGATCATGCTGAACTCCTTGCATAAGTATGAGCCTCGAATCCACATAGTGAGAGTTGGGGGTCCACAGCGCATGATCACCAGCCACTGCTTCCCTGAGACCCAGTTCATAGCGGTGACTGCTTATCAGAACGAGGAGATCACAGCTCTTAAAATTAAGTACAATCCATTTGCAAAAGCTTTCCTTGATGCAAAGGAAAGAAGTGATCACAAAGAGATGATGGAGGAACCCGGAGACAGCCAGCAACCTGGGTACTCCCAATCCTATTCTGACAACTCACCTGCATGTTTATCCATGCTGCAATCCCATGACAATTGGTCCAGCCTTGGAATGCCTGCCCATCCCAGCATGCTCCCCGTGAGCCACAATGCCAGCCCACCTACCAGCTCCAGTCAGTACCCCAGCCTGTGGTCTGTGAGCAACGGCGCCGTCACCCCGGGCTCCCAGGCAGCAGCCGTGTCCAACGGGCTGGGGGCCCAGTTCTTCCGGGGCTCCCCCGCGCACTACACACCCCTCACCCATCCGGTCTCGGCGCCCTCTTCCTCGGGATCCCCACTGTACGAAGGGGCGGCCGCGGCCACAGACATCGTGGACAGCCAGTACGACGCCGCAGCCCAAGGCCGCCTCATAGCCTCATGGACACCTGTGTCGCCACCTTCCATGTGAAGCAGCAAGGCCCAGGTCCCGAAAGATGCAGTGACTTTTTGTCGTGGCAGCCAGTGGTGACTGGATTGACCTACTAGGTACCCAGTGGCAGTCTCAGGTTAAGAAGGAAATGCAGCCTCAGTAACTTCCTTTTCAAAGCAGTGGAGGAGCACACGGCACCTTTCCCCAGAGCCCCAGCATCCCTTGCTCACACCTGCAGTAGCGGTGCTGTCCCAGGTGGCTTACAGATGAACCCAACTGTGGAGATGATGCAGTTGGCCCAACCTCACTGACGGTGAAAAAATGTTTGCCAGGGTCCAGAAACTTTTTTTGGTTTATTTCTCATACAGTGTATTGGCAACTTTGGCACACCAGAATTTGTAAACTCCACCAGTCCTACTTTAGTGAGATAAAAAGCACACTCTTAATCTTCTTCCTTGTTGCTTTCAAGTAGTTAGAGTTGAGCTGTTAAGGACAGAATAAAATCATAGTTGAGGACAGCAGGTTTTAGTTGAATTGAAAATTTGACTGCTCTGCCCCCTAGAATGTGTGTATTTTAAGCATATGTAGCTAATCTCTTGTGTTGTTAAACTATAACTGTTTCATATTTTTCTTTTGACAAAGTAGCCAAAGACAATCAGCAGAAAGCATTTTCTGCAAAATAAACGCAATATGCAAAA |