Mutations on the Protein: P12235 From Positions: 89 To 104
Swiss-Prot Disease: VAR_038814 
p.ALA90ASP
N/A
| |
N/A
|
|---|
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 2 (PEOA2)
|
|---|
Swiss-Prot Disease: VAR_022460 
p.ASP104GLY
N/A
| |
N/A
|
|---|
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 2 (PEOA2)
|
|---|
Swiss-Prot Disease: VAR_022459 
p.LEU98PRO
N/A
| |
N/A
|
|---|
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 2 (PEOA2)
|
|---|
OMIM Disease: 103220.0004 
p.ASP104GLY
N/A
| |
N/A
|
|---|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,||AUTOSOMAL DOMINANT, 2
|
|---|
OMIM Disease: 103220.0003 
p.LEU98PRO
N/A
| |
N/A
|
|---|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,||AUTOSOMAL DOMINANT, 2
|
|---|
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 |
|
5
3
0
2