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Symbol
Name
ID

Dnm1l
dynamin 1-like
MGI:1921256

Phenotype annotations related to vision/eye

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	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
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
Availability	Mouse Genotype
	Dnm1l^{tm1b(KOMP)Wtsi}/Dnm1l⁺

Contributing Projects: 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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