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Known Diseases associated with this Protein: |  FACIAL PARESIS, HEREDITARY CONGENITAL, 3
| FACIAL PARESIS, HEREDITARY CONGENITAL, 3 (HCFP3)
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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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| Swiss-Prot | VAR_068723 | Disease | p.ARG207CYS | Facial paresis, hereditary congenital, 3 (HCFP3) | | dbSNP | rs12939811 | Polymorphism | p.GLN103HIS | N/A | | dbSNP | rs7226137 | Polymorphism | p.GLU265GLY | N/A | | Swiss-Prot | VAR_055959 | Polymorphism | p.THR71ASN | N/A | | OMIM | 142968.0001 | Disease | p.ARG207CYS | FACIAL PARESIS, HEREDITARY CONGENITAL, 3 |
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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251757285
HXB1_HUMAN RecName: Full=Homeobox protein Hox-B1; AltName: Full=Homeobox protein Hox-2I
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