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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_000643 | Disease | p.LYS78GLU | Hyperalphalipoproteinemia 2 (HALP2) | | Swiss-Prot | VAR_000644 | Polymorphism | p.THR94ALA | N/A | | OMIM | 107720.0003 | Disease | p.ARG19TER | HYPERALPHALIPOPROTEINEMIA 2 | | OMIM | 107720.0002 | Disease | p.LYS58GLU | HYPERALPHALIPOPROTEINEMIA 2 | | OMIM | 107720.0001 | Disease | p.THR74ALA | APOLIPOPROTEIN C-III, NONGLYCOSYLATED |
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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114026
APOC3_HUMAN RecName: Full=Apolipoprotein C-III; Short=Apo-CIII; Short=ApoC-III; AltName: Full=Apolipoprotein C3; Flags: Precursor
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