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Known Diseases associated with this Protein: |  ALPORT SYNDROME, WITH MACROTHROMBOCYTOPENIA (APSM)
| DEAFNESS, AUTOSOMAL DOMINANT 17
| DEAFNESS, AUTOSOMAL DOMINANT, 17 (DFNA17)
| EPSTEIN SYNDROME
| EPSTEIN SYNDROME (EPS)
| EPSTEIN SYNDROME, INCLUDED
| EPSTEIN SYNDROME, INCLUDED;;
| FECHTNER SYNDROME
| FECHTNER SYNDROME (FTNS)
| FECHTNER SYNDROME, INCLUDED
| FECHTNER SYNDROME, INCLUDED;;
| MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS, INCLUD
| MAY-HEGGLIN ANOMALY
| MAY-HEGGLIN ANOMALY (MHA)
| MAY-HEGGLIN ANOMALY, INCLUDED
| SEBASTIAN SYNDROME
| SEBASTIAN SYNDROME (SBS)
| SEBASTIAN SYNDROME, INCLUDED
| SEBASTIAN SYNDROME, INCLUDED;;
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|  | Tips: The Domains on the Default View are decided by HMMER's search E-Value of the Protein against the Domain model. Clicking a check box on the left will display or hide the corresponding domain(s). To view the Protein page, either click on the protein links in the box to the left or the blue bar above the Protein's graphic. |
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Domains found on the Proteins
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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MYH9
4627
28
4
11
1
20
