Species: Hu, Mu, RM
Applications: WB, ICC/IF, IHC, IP
Host: Rabbit Polyclonal
Species: Hu
Applications: WB, ELISA, ICC/IF, IP
Host: Mouse Monoclonal
Species: Hu, Mu, Rt
Applications: WB
Host: Rabbit Polyclonal
Species: Hu
Applications: WB
Species: Hu
Applications: AC
Description
WBSCR22 encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
Bioinformatics
| Entrez |
Human
|
| Uniprot |
Human
Human
Human
Human
|
| Product By Gene ID |
114049 |
| Alternate Names |
- EC 2.1.1.-
- FLJ44236
- HASJ4442
- HUSSY-3
- MGC19709
- MGC2022
- MGC5140
- PP3381
- WBMT
- Williams Beuren syndrome chromosome region 22 protein
- Williams Beuren syndrome chromosome region 22
- Williams-Beuren candidate region putative methyltransferase
- Williams-Beuren syndrome chromosomal region 22 protein
|
