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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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Domains found on the Protein Table of Mutations found on the ProteinSource ↕ | Mut_ID ↕ | Class ↕ | HGVS ↕ | Disease ↕ |
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OMIM | 603273.0006 | Disease | p.ARG186CYS | SPLIT-HAND/FOOT MALFORMATION 4 | OMIM | 603273.0002 | Disease | p.ARG110GLN | ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3 | OMIM | 603273.0024 | Disease | p.ARG133GLN | ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3||ADULT SYNDROME, INCLUDED | OMIM | 603273.0014 | Disease | p.ARG204GLN | ADULT SYNDROME | OMIM | 603273.0008 | Disease | p.ARG210GLN | ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3 | OMIM | 603273.0022 | Disease | p.ARG204GLY | ADULT SYNDROME | OMIM | 603273.0021 | Disease | p.ARG219GLY | OROFACIAL CLEFT 8 | OMIM | 603273.0007 | Disease | p.ARG185HIS | ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3||RAPP-HODGKIN SYNDROME, INCLUDED | OMIM | 603273.0028 | Disease | p.ARG133PRO | ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3 | OMIM | 603273.0019 | Disease | p.ARG451PRO | RAPP-HODGKIN SYNDROME | OMIM | 603273.0001 | Disease | p.ARG110TRP | ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3 | OMIM | 603273.0015 | Disease | p.ASP218GLY | ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3 | OMIM | 603273.0003 | Disease | p.CYS212ARG | ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME||3 | OMIM | 603273.0010 | Disease | p.CYS428GLY | ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE | OMIM | 603273.0018 | Disease | p.ILE416THR | ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE||RAPP-HODGKIN SYNDROME, INCLUDED | OMIM | 603273.0009 | Disease | p.LEU420PHE | ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE | OMIM | 603273.0005 | Disease | p.LYS100GLU | SPLIT-HAND/FOOT MALFORMATION 4 | OMIM | 603273.0026 | Disease | p.PRO33LEU | ADULT SYNDROME | OMIM | 603273.0020 | Disease | p.VAL20MET | ADULT SYNDROME |
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
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