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Symbol
Name
ID

Nsun2
NOL1/NOP2/Sun domain family member 2
MGI:107252

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Hypertelorism	Hypotelorism	Strabismus	Horizontal nystagmus
Disease(s) Associated with NSUN2
autosomal recessive intellectual developmental disorder 5

Mouse Phenotypes		abnormal eye muscle morphology	abnormal optic chiasm morphology	abnormal cornea morphology	abnormal lens morphology	cataract	abnormal optic cup morphology	abnormal optic stalk morphology	excessive tearing
Availability	Mouse Genotype	abnormal eye muscle morphology	abnormal optic chiasm morphology	abnormal cornea morphology	abnormal lens morphology	cataract	abnormal optic cup morphology	abnormal optic stalk morphology	excessive tearing
	Nsun2^{tm1a(EUCOMM)Wtsi}/Nsun2^{tm1a(EUCOMM)Wtsi}
	Nsun2^{tm1a(EUCOMM)Wtsi}/Nsun2⁺

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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