Fbxo22 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fbxo22
F-box protein 22
MGI:1926014

10 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fbxo22^em1Mkt/Fbxo22^em1Mkt involves: C57BL/6N	abnormal cell physiology	J:236274
	decreased fibroblast proliferation	J:236274
	postnatal lethality, incomplete penetrance	J:236274
Fbxo22^{tm1b(EUCOMM)Wtsi}/Fbxo22⁺ C57BL/6N-Fbxo22^{tm1b(EUCOMM)Wtsi}/Nju	decreased heart left ventricle size	J:211773
	thin ventricular wall	J:211773
Fbxo22^{tm1b(EUCOMM)Wtsi}/Fbxo22^{tm1b(EUCOMM)Wtsi} C57BL/6N-Fbxo22^{tm1b(EUCOMM)Wtsi}/Nju	abnormal tail morphology	J:211773
	decreased grip strength	J:211773
	decreased prepulse inhibition	J:211773
	female infertility	J:211773
	male infertility	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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