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Known Diseases associated with this Protein: |  ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED
| TOOTH AGENESIS, SELECTIVE, X-LINKED, 1
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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 Table of Mutations found on the Protein| Source ↕ | Mut_ID ↕ | Class ↕ | HGVS ↕ | Disease ↕ |
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| OMIM | 300451.0010 | Disease | p.ALA347THR | ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED | | OMIM | 300451.0005 | Disease | p.ARG155CYS | ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED | | OMIM | 300451.0006 | Disease | p.ARG156CYS | ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED | | OMIM | 300451.0019 | Disease | p.ARG276CYS | ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED | | OMIM | 300451.0014 | Disease | p.ARG65GLY | TOOTH AGENESIS, SELECTIVE, X-LINKED, 1 | | OMIM | 300451.0007 | Disease | p.ARG156HIS | ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED | | OMIM | 300451.0002 | Disease | p.ARG69LEU | ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED | | OMIM | 300451.0015 | Disease | p.GLN356GLU | TOOTH AGENESIS, SELECTIVE, X-LINKED, 1 | | OMIM | 300451.0003 | Disease | p.GLN23TER | ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED | | OMIM | 300451.0004 | Disease | p.GLU63LYS | ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED | | OMIM | 300451.0009 | Disease | p.GLY224ALA | ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED | | OMIM | 300451.0008 | Disease | p.PRO209LEU | ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED | | OMIM | 300451.0018 | Disease | p.THR336MET | TOOTH AGENESIS, SELECTIVE, X-LINKED, 1 | | OMIM | 300451.0001 | Disease | p.TYR61HIS | ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED | | OMIM | 300451.0011 | Disease | p.TYR61TER | ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED |
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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54112101
ectodysplasin-A isoform 2 [Homo sapiens]
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