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)
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