|  | 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 | Domain ↕ | CD Accession ↕ | E-Value ↕ | Start ↕ | End ↕ |
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Table of Mutations found on the Protein| Source ↕ | Mut_ID ↕ | Class ↕ | HGVS ↕ | Disease ↕ |
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| dbSNP | rs1563632 | Polymorphism | p.ARG556HIS | N/A | | dbSNP | rs12449313 | Polymorphism | p.ASN636SER | N/A | | dbSNP | rs73291850 | Polymorphism | p.GLY593CYS | N/A | | dbSNP | rs9911649 | Polymorphism | p.GLY553GLU | N/A | | dbSNP | rs8080966 | Polymorphism | p.PRO524LEU | N/A |
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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147733168
SMCR8_HUMAN RecName: Full=Smith-Magenis syndrome chromosomal region candidate gene 8 protein
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