Nsun5 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Nsun5
NOL1/NOP2/Sun domain family, member 5
MGI:2140844

20 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nsun5^em1Lgch/Nsun5^em1Lgch involves: C57BL/6J	abnormal dentate gyrus morphology	J:271670
	abnormal excitatory postsynaptic potential	J:271670
	abnormal spatial working memory	J:271670
	impaired spatial learning	J:271670
	normal nervous system phenotype	J:271670
	reduced long-term potentiation	J:271670
Nsun5^{tm2b(EUCOMM)Wtsi}/Nsun5^{tm2b(EUCOMM)Wtsi} C57BL/6N-Nsun5^{tm2b(EUCOMM)Wtsi}/J	abnormal behavior	J:211773
	decreased locomotor activity	J:211773
	decreased lymphocyte cell number	J:211773
	decreased spleen weight	J:211773
	decreased thigmotaxis	J:211773
	increased fasting circulating glucose level	J:211773
	increased neutrophil cell number	J:211773
	prolonged QRS complex duration	J:211773
	thrombocytopenia	J:211773
Nsun5^{tm2b(EUCOMM)Wtsi}/Nsun5^{tm2b(EUCOMM)Wtsi} C57BL/6NJ-Nsun5^{tm2b(EUCOMM)Wtsi}/J	decreased erythrocyte cell number	J:211773
	decreased hematocrit	J:211773
	decreased hemoglobin content	J:211773
	impaired pupillary reflex	J:211773
	increased circulating alanine transaminase level	J:211773
	thrombocytopenia	J:211773

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 11/12/2024 MGI 6.24