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Symbol Name ID |
mt-Nd6
mitochondrially encoded NADH dehydrogenase 6 MGI:102495 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Central retinal vessel vascular tortuosity |
Cataract |
Abnormal optic nerve morphology |
Optic atrophy |
Leber optic atrophy |
Optic neuropathy |
Pigmentary retinopathy |
Strabismus |
Nystagmus |
Ophthalmoplegia |
Centrocecal scotoma |
Visual loss |
Ptosis |
| Disease(s) Associated with ND6 | |||||||||||||
| Leber hereditary optic neuropathy | |||||||||||||
| Leigh disease |
| Mouse Phenotypes | vision/eye phenotype |
abnormal retina ganglion cell morphology |
abnormal optic nerve morphology |
decreased a-wave amplitude |
decreased b-wave amplitude |
abnormal eye electrophysiology |
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| Availability | Mouse Genotype | ||||||
| mt-Nd6m2Jiha | * | ||||||
| mt-Nd6m3Dwa | |||||||
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 04/30/2024 MGI 6.23 |
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