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Symbol
Name
ID
Nsun2
NOL1/NOP2/Sun domain family member 2
MGI:107252
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Achilles tendon contracture
Hypertonia
Spasticity
Hypotonia
Axial hypotonia
Disease(s) Associated with NSUN2
autosomal recessive intellectual developmental disorder 5

Mouse Phenotypes
abnormal eye muscle morphology
abnormal infrahyoid muscle connection
Availability Mouse Genotype
Nsun2tm1a(EUCOMM)Wtsi/Nsun2tm1a(EUCOMM)Wtsi

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory