TBXT
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 6[14]
- Cytogenetic location
- 6q27[18]
- Encodes
- T-box transcription factor T, Brachyury protein[11][12]
- Expressed in
- gonad, testicle, oocyte, pars reticulata, renal medulla, synovial joint, secondary oocyte, human penis, external globus pallidus, synovial membrane[19][20][21][22][23][24][25][26][27][28]
- Found in taxon
- Homo sapiens[13]
- Genetic association
- chordoma, sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome[15][16]
- HomoloGene ID
- 2393[3]
- Strand orientation
- reverse strand[17]
🏷️ Also known as
en TFT
en SAVA
en T
en T-box transcription factor T
en T, brachyury homolog (mouse)
en T brachyury transcription factor
en TBXT
ar براتشيوري
ja ブラキウリ
ru Brachyury
🔖 Identifiers · 13
- OpenAlex ID
- C46122727
- Image (Wikimedia Commons)
- PDB 1xbr EBI.jpg ↗
- Ensembl gene ID
- ENSG00000164458
- Ensembl transcript ID
- ENST00000461348, ENST00000296946, ENST00000366871, ENST00000366876
- Entrez Gene ID
- 6862
- Exact match
- identifiers.org
- Freebase ID
- /m/09rfz6
- HGNC ID
- 11515
- HGNC gene symbol
- TBXT
- Microsoft Academic ID (discontinued)
- 46122727
- OMIM ID
- 601397
- RefSeq RNA ID
- NM_001270484, NM_003181, NM_001366285, NM_001366286, XM_047419269
Show all 13 identifiers +1
- UMLS CUI
- C1420562
🔗 Connections
Expressed in 7
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
← Genetic association 1
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