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Known Diseases associated with this Protein: |  MARTSOLF SYNDROME
| MARTSOLF SYNDROME (MARTS)
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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_029881 | Disease | p.GLY1052CYS | Martsolf syndrome (MARTS) | | dbSNP | rs11547779 | Polymorphism | p.LEU1165PHE | N/A | | dbSNP | rs2289189 | Polymorphism | p.SER1092THR | N/A | | dbSNP | rs12045447 | Polymorphism | p.THR863ALA | N/A | | OMIM | 609275.0001 | Disease | p.GLY1051CYS | MARTSOLF SYNDROME |
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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62511132
RBGPR_HUMAN RecName: Full=Rab3 GTPase-activating protein non-catalytic subunit; AltName: Full=RGAP-iso; AltName: Full=Rab3 GTPase-activating protein 150 kDa subunit; AltName: Full=Rab3-GAP p150; Short=Rab3-GAP150; AltName: Full=Rab3-GAP regulatory subunit
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