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Symbol Name ID |
Ndufa1
NADH:ubiquinone oxidoreductase subunit A1 MGI:1929511 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frequent falls |
Cerebellar atrophy |
Ataxia |
Choreoathetosis |
Myoclonus |
Aphasia |
Delayed speech and language development |
Dementia |
Intellectual disability |
Hyporeflexia |
Gait imbalance |
Unsteady gait |
Global developmental delay |
Delayed ability to walk |
Seizure |
Bilateral tonic-clonic seizure |
Generalized myoclonic seizure |
| Disease(s) Associated with NDUFA1 | |||||||||||||||||
| nuclear type mitochondrial complex I deficiency 12 |
| Mouse Phenotypes | Purkinje cell degeneration |
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| Availability | Mouse Genotype | |
| Ndufa1tm1.1Nay/Y | ||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 08/02/2024 MGI 6.24 |
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