|
|
|---|
 |
|
Known Diseases associated with this Protein: |  HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4
|
|  | Tips: The Domains on the Default View are decided by the Domain's E-Value. Clicking a check box will display or hide the correlated domain. To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic. |
|---|
 Default View:
| |
|---|
Domains found on the Protein Table of Mutations found on the Protein| Source ↕ | Mut_ID ↕ | Class ↕ | HGVS ↕ | Disease ↕ |
|---|
| dbSNP | rs17073498 | Polymorphism | p.ARG49GLN | N/A | | Swiss-Prot | VAR_011995 | Polymorphism | p.GLU31GLN | N/A | | Swiss-Prot | VAR_011996 | Polymorphism | p.LEU204HIS | N/A | | dbSNP | rs9496891 | Polymorphism | p.THR277ALA | N/A | | OMIM | 605014.0003 | Disease | p.GLN268TER | HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4 |
Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.
| DMDM_info@umbc.edu | 1000 Hilltop Circle, Baltimore, MD
21250 | Department of Biological Sciences | Phone: 410-455-2258 |
|
6175047
STX11_HUMAN RecName: Full=Syntaxin-11
1
4
1
2
2
