Known Diseases associated with this Protein: |  CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IS
| VARIANT OF UNKNOWN SIGNIFICANCE
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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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| OTU | pfam02338 | 7.6e-25 | 133 | 242 |
Table of Mutations found on the Protein| Source ↕ | Mut_ID ↕ | Class ↕ | HGVS ↕ | Disease ↕ |
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| OMIM | 300776.0002 | Disease | p.ASN3SER | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Is | | OMIM | 300776.0003 | Disease | p.THR37LEU | VARIANT OF UNKNOWN SIGNIFICANCE |
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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380848759
UDP-N-acetylglucosamine transferase subunit ALG13 homolog isoform 5 [Homo sapiens]
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