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Known Diseases associated with this Protein: |  MEIER-GORLIN SYNDROME 3
| MEIER-GORLIN SYNDROME 3 (MGORS3)
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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 | 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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| Swiss-Prot | VAR_029283 | Polymorphism | p.ARG32TRP | N/A | | Swiss-Prot | VAR_029284 | Polymorphism | p.PRO138GLN | N/A | | Swiss-Prot | VAR_065487 | Disease | p.TYR232SER | Meier-Gorlin syndrome 3 (MGORS3) | | OMIM | 607213.0002 | Disease | p.TYR232SER | MEIER-GORLIN SYNDROME 3 |
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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8928274
ORC6_HUMAN RecName: Full=Origin recognition complex subunit 6
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