Nrgn Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Nrgn
neurogranin
MGI:1927184

11 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nrgn^em1(IMPC)H/Nrgn^em1(IMPC)H C57BL/6NTac-Nrgn^em1(IMPC)H/H	abnormal locomotor behavior	J:211773
	decreased circulating amylase level	J:211773
	increased circulating serum albumin level	J:211773
Nrgn^tm1Kph/Nrgn⁺ involves: 129/Sv * C57BL/6	abnormal contextual conditioning behavior	J:65166
Nrgn^tm1Kph/Nrgn⁺ involves: 129/Sv * C57BL/6	abnormal spatial learning	J:65166
Nrgn^tm1Kph/Nrgn^tm1Kph involves: 129/Sv * C57BL/6	abnormal long-term potentiation	J:65166
	abnormal spatial learning	J:65166
	impaired synaptic plasticity	J:65166
Nrgn^tm1Sut/Nrgn^tm1Sut involves: 129S4/SvJae * Black Swiss	abnormal excitatory postsynaptic potential	J:109224
	abnormal long-term depression	J:109224
	enhanced long-term potentiation	J:109224
	increased post-tetanic potentiation	J:109224

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 12/10/2024 MGI 6.24