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Known Diseases associated with this Protein: |  ACROMESOMELIC CHONDRODYSPLASIA, GREBE TYPE (AMDG)
| BRACHYDACTYLY A1, C (BDA1C)
| BRACHYDACTYLY A2 (BDA2)
| BRACHYDACTYLY C (BDC)
| BRACHYDACTYLY, TYPE A1, C
| BRACHYDACTYLY, TYPE A2
| BRACHYDACTYLY, TYPE A2, INCLUDED
| BRACHYDACTYLY, TYPE C
| CHONDRODYSPLASIA, GREBE TYPE
| DU PAN SYNDROME (DPS)
| FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY
| MULTIPLE SYNOSTOSES SYNDROME 2
| MULTIPLE SYNOSTOSES SYNDROME 2 (SYNS2)
| MULTIPLE SYNOSTOSES SYNDROME 2, INCLUDED
| SYMPHALANGISM, PROXIMAL 1B (SYM1B)
| SYMPHALANGISM, PROXIMAL, 1B
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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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 Default View:
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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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GDF5
8200
26
4
13
3
14
