Sh3rf1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Sh3rf1
SH3 domain containing ring finger 1
MGI:1913066

16 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Sh3rf1^em1(IMPC)J/Sh3rf1^em1(IMPC)J C57BL/6NJ-Sh3rf1^em1(IMPC)J/Mmjax	abnormal optic disk morphology	J:211773
	decreased exploration in new environment	J:211773
Sh3rf1^em1Bcgen/Sh3rf1^em1Bcgen Tg(Nes-cre)1Kln/0 involves: C57BL/6 * SJL	abnormal nest building behavior	J:326378
	abnormal spatial reference memory	J:326378
	decreased body weight	J:326378
	decreased excitatory postsynaptic current amplitude	J:326378
	decreased social investigation	J:326378
	decreased vocalization	J:326378
	hypoactivity	J:326378
	impaired contextual conditioning behavior	J:326378
	impaired spatial learning	J:326378
	increased stereotypic behavior	J:326378
	reduced long-term potentiation	J:326378
	normal taste/olfaction phenotype	J:326378
Sh3rf1^em1Bcgen/Sh3rf1^em1Bcgen Tg(Nes-cre)1Kln/0 Tg(Thy1-EGFP)MJrs/0 involves: C57BL/6 * CBA * SJL	decreased dendritic spine density	J:326378
	decreased dendritic spine length	J:326378

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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