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Known Diseases associated with this Protein: |  NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
| NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A, SEVERE
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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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| OMIM | 300110.0004 | Disease | p.ARG765TER | NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A | | OMIM | 300110.0002 | Disease | p.ARG893TER | NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A | | OMIM | 300110.0001 | Disease | p.GLY304ASP | NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A | | OMIM | 300110.0006 | Disease | p.ILE680THR | NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A, SEVERE |
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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377823713
voltage-dependent L-type calcium channel subunit alpha-1F isoform 3 [Homo sapiens]
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