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Known Diseases associated with this Protein: | EPILEPSY, NOCTURNAL FRONTAL LOBE, 5
| EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14
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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 ProteinSource ↕ | Mut_ID ↕ | Class ↕ | HGVS ↕ | Disease ↕ |
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OMIM | 608167.0002 | Disease | p.ALA934THR | EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14 | OMIM | 608167.0005 | Disease | p.ARG928CYS | EPILEPSY, NOCTURNAL FRONTAL LOBE, 5 | OMIM | 608167.0007 | Disease | p.ARG398GLN | EPILEPSY, NOCTURNAL FRONTAL LOBE, 5 | OMIM | 608167.0001 | Disease | p.ARG428GLN | EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14 | OMIM | 608167.0003 | Disease | p.ARG474HIS | EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14 | OMIM | 608167.0004 | Disease | p.ILE760MET | EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14 | OMIM | 608167.0008 | Disease | p.MET896ILE | EPILEPSY, NOCTURNAL FRONTAL LOBE, 5 | OMIM | 608167.0009 | Disease | p.PHE932ILE | EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14 | OMIM | 608167.0006 | Disease | p.TYR796HIS | EPILEPSY, NOCTURNAL FRONTAL LOBE, 5 |
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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