Symbol Name ID |
Dnm1l
dynamin 1-like MGI:1921256 |
Darker colors indicate more annotations |
Human Phenotypes | Optic atrophy |
Optic disc pallor |
Deeply set eye |
Abnormality of pattern visual evoked potentials |
Strabismus |
Horizontal nystagmus |
Oculomotor apraxia |
Tritanomaly |
Constriction of peripheral visual field |
Central scotoma |
Slow decrease in visual acuity |
Disease(s) Associated with DNM1L | |||||||||||
encephalopathy due to defective mitochondrial and peroxisomal fission 1 | |||||||||||
optic atrophy 5 |
Mouse Phenotypes | abnormal optic disk morphology |
abnormal cornea morphology |
persistence of hyaloid vascular system |
abnormal vitreous body morphology |
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Availability | Mouse Genotype | ||||
Dnm1ltm1b(KOMP)Wtsi/Dnm1l+ |
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 03/12/2024 MGI 6.23 |
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