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Known Diseases associated with this Protein: |  DYSTONIA 8 (DYT8)
| PAROXYSMAL NONKINESIGENIC DYSKINESIA 1
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|  | 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. |
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 Default View:
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Domains found on the Protein Table of Mutations found on the Protein| Source ↕ | Mut_ID ↕ | Class ↕ | HGVS ↕ | Disease ↕ |
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| Swiss-Prot | VAR_034844 | Disease | p.ALA7VAL | Dystonia 8 (DYT8) | | Swiss-Prot | VAR_034845 | Disease | p.ALA9VAL | Dystonia 8 (DYT8) | | dbSNP | rs73990423 | Polymorphism | p.ARG152GLN | N/A | | OMIM | 609023.0003 | Disease | p.ALA33PRO | PAROXYSMAL NONKINESIGENIC DYSKINESIA 1 | | OMIM | 609023.0002 | Disease | p.ALA7VAL | PAROXYSMAL NONKINESIGENIC DYSKINESIA 1 | | OMIM | 609023.0001 | Disease | p.ALA9VAL | PAROXYSMAL NONKINESIGENIC DYSKINESIA 1 |
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 |
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158563846
PNKD_HUMAN RecName: Full=Probable hydrolase PNKD; AltName: Full=Myofibrillogenesis regulator 1; Short=MR-1; AltName: Full=Paroxysmal nonkinesiogenic dyskinesia protein; AltName: Full=Trans-activated by hepatitis C virus core protein 2
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