Species: Hu, Mu, Rt
Applications: WB, ICC/IF, IHC, ChIP
Host: Rabbit Polyclonal
Species: Hu, Mu
Applications: WB, ICC/IF, IHC, IP
Host: Rabbit Polyclonal
Species: Hu, Mu
Applications: WB, ELISA, ICC/IF, IHC
Host: Mouse Monoclonal
Species: Hu
Applications: WB, ELISA, MA, PAGE, AP
Species: Hu
Applications: WB, ELISA, MA, PAGE, AP
Species: Hu
Applications: AC
Description
TFII-I encodes a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. The exon(s) encoding 5' UTR has not been fully defined, but this gene is known to contain at least 34 exons, and its alternative splicing generates 4 transcript variants.
Bioinformatics
| Entrez |
Human
|
| Uniprot |
Human
Human
Human
Human
Human
|
| Product By Gene ID |
2969 |
| Alternate Names |
- BAP-135,135kD
- BAP135WBS
- Bruton tyrosine kinase-associated protein 135
- BTKAP1
- DIWS
- FLJ38776
- FLJ56355
- general transcription factor II, i
- general transcription factor IIi
- general transcription factor II-I
- GTFII-I
- IB291
- SPINBTK-associated protein 135
- TFII-ISRF-Phox1-interacting protein
- WBSCR6
- Williams-Beuren syndrome chromosome region 6
|
