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Symbol
Name
ID

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

Phenotype annotations related to integument

Darker colors indicate more annotations

Human Phenotypes	Synophrys	Thick eyebrow	Eczematoid dermatitis	Sparse hair
Disease(s) Associated with NSUN2
autosomal recessive intellectual developmental disorder 5

Mouse Phenotypes		subcutaneous edema	abnormal coat appearance	alopecia	disheveled coat	abnormal hair cycle	abnormal hair cycle anagen phase	abnormal hair shedding	abnormal epidermis stratum basale morphology
Availability	Mouse Genotype	subcutaneous edema	abnormal coat appearance	alopecia	disheveled coat	abnormal hair cycle	abnormal hair cycle anagen phase	abnormal hair shedding	abnormal epidermis stratum basale morphology
	Nsun2^{Gt(D014D11)Wrst}/Nsun2^{Gt(D014D11)Wrst}
	Nsun2^{tm1a(EUCOMM)Wtsi}/Nsun2^{tm1a(EUCOMM)Wtsi}
	Nsun2^{tm1a(EUCOMM)Wtsi}/Nsun2⁺
	Nsun2^{tm1c(EUCOMM)Wtsi}/Nsun2^{tm1c(EUCOMM)Wtsi} Tg(KRT14-cre)1Amc/? (conditional)

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23