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Known Diseases associated with this Protein: |  DEAFNESS, AUTOSOMAL DOMINANT 13
| DEAFNESS, AUTOSOMAL DOMINANT, 13 (DFNA13)
| DEAFNESS, AUTOSOMAL RECESSIVE 53
| DEAFNESS, AUTOSOMAL RECESSIVE, 53 (DFNB53)
| OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA
| OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA (OSMED)
| OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA, HETEROZYGOUS, INCLUDED
| STICKLER SYNDROME, TYPE III
| WEISSENBACHER-ZWEYMUELLER SYNDROME (WZS)
| WEISSENBACHER-ZWEYMULLER SYNDROME
| WEISSENBACHER-ZWEYMULLER SYNDROME, AUTOSOMAL RECESSIVE
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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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COL11A2
1302
13
20
8
10
15
