Known Diseases associated with this Protein: |  MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C
| VARIANT OF UNKNOWN SIGNIFICANCE
|
|  | 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 ↕ |
|---|
| OMIM | 603930.0002 | Disease | p.ASN10TYR | VARIANT OF UNKNOWN SIGNIFICANCE | | OMIM | 603930.0003 | Disease | p.ASP580ALA | MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C |
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 |
|
10880983
gephyrin isoform 1 [Homo sapiens]
2
0
2
0
0
