Known Diseases associated with this Protein: |  OSTEOGENESIS IMPERFECTA, TYPE VIII
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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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| P4Hc | smart00702 | 1.2e-59 | 469 | 677 |
Table of Mutations found on the Protein| Source ↕ | Mut_ID ↕ | Class ↕ | HGVS ↕ | Disease ↕ |
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| OMIM | 610339.0006 | Disease | p.ARG368TER | OSTEOGENESIS IMPERFECTA, TYPE VIII | | OMIM | 610339.0004 | Disease | p.TYR552TER | OSTEOGENESIS IMPERFECTA, TYPE VIII |
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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342837704
prolyl 3-hydroxylase 1 isoform 3 precursor [Homo sapiens]
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