Symbol Name ID |
Nsun2
NOL1/NOP2/Sun domain family member 2 MGI:107252 |
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 |
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Availability | Mouse Genotype | ||||||||
Nsun2tm1a(EUCOMM)Wtsi/Nsun2tm1a(EUCOMM)Wtsi | |||||||||
Nsun2tm1a(EUCOMM)Wtsi/Nsun2+ |
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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