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Known Diseases associated with this Protein: |  SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT
| SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT (SPG33)
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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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| dbSNP | rs10882993 | Polymorphism | p.GLY138VAL | N/A | | dbSNP | rs35077384 | Disease | p.GLY191VAL | Spastic paraplegia 33, autosomal dominant (SPG33) | | dbSNP | rs17108378 | Polymorphism | p.VAL82ILE | N/A | | OMIM | 610243.0001 | Disease | p.GLY191VAL | SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT |
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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74744927
ZFY27_HUMAN RecName: Full=Protrudin; AltName: Full=Zinc finger FYVE domain-containing protein 27
2
2
1
3
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