Nrgn Phenotype Annotations

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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)
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