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Known Diseases associated with this Protein: |  LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
| MITOCHONDRIAL COMPLEX I DEFICIENCY
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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 | 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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| Swiss-Prot | VAR_012037 | Polymorphism | p.THR174PRO | N/A | | OMIM | 602694.0003 | Disease | p.ARG106TER | LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY | | OMIM | 602694.0004 | Disease | p.TRP15TER | MITOCHONDRIAL COMPLEX I DEFICIENCY | | OMIM | 602694.0002 | Disease | p.TRP96TER | MITOCHONDRIAL COMPLEX I DEFICIENCY |
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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3287881
NDUS4_HUMAN RecName: Full=NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial; AltName: Full=Complex I-18 kDa; Short=CI-18 kDa; AltName: Full=Complex I-AQDQ; Short=CI-AQDQ; AltName: Full=NADH-ubiquinone oxidoreductase 18 kDa subunit; Flags: Precursor
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