Known Diseases associated with this Protein: |  FOCAL DERMAL HYPOPLASIA
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 Default View:
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Domains found on the Protein | Domain ↕ | CD Accession ↕ | E-Value ↕ | Start ↕ | End ↕ |
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Table of Mutations found on the Protein| Source ↕ | Mut_ID ↕ | Class ↕ | HGVS ↕ | Disease ↕ |
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| OMIM | 300651.0005 | Disease | p.ARG359GLN | FOCAL DERMAL HYPOPLASIA | | OMIM | 300651.0003 | Disease | p.ARG124TER | FOCAL DERMAL HYPOPLASIA | | OMIM | 300651.0004 | Disease | p.TRP74TER | FOCAL DERMAL HYPOPLASIA |
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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45439333
protein-cysteine N-palmitoyltransferase porcupine isoform C [Homo sapiens]
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