Symbol Name ID |
Ndufs4
NADH:ubiquinone oxidoreductase core subunit S4 MGI:1343135 |
Darker colors indicate more annotations |
Human Phenotypes | Cataract |
Abnormal optic nerve morphology |
Optic atrophy |
Pigmentary retinopathy |
Strabismus |
Nystagmus |
Ophthalmoplegia |
Ptosis |
Disease(s) Associated with NDUFS4 | ||||||||
Leigh disease |
Mouse Phenotypes | optic nerve atrophy |
cataract |
blepharoptosis |
abnormal eye electrophysiology |
abnormal vision |
blindness |
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Availability | Mouse Genotype | ||||||
Ndufs4tm1.1Rpa/Ndufs4tm1.1Rpa | |||||||
Ndufs4tm1Rpa/Ndufs4tm1Rpa Tg(Nes-cre)1Kln/0 (conditional) |
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 04/23/2024 MGI 6.23 |
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