Fbxo42 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fbxo42
F-box protein 42
MGI:1924992

13 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Fbxo42^em1(IMPC)J/Fbxo42⁺ C57BL/6NJ-Fbxo42^em1(IMPC)J/Mmjax	abnormal auditory brainstem response	J:211773
	decreased circulating alanine transaminase level	J:211773
	decreased circulating aspartate transaminase level	J:211773
	decreased circulating bilirubin level	J:211773
	increased circulating calcium level	J:211773
	prolonged QRS complex duration	J:211773
	thrombocytosis	J:211773
Fbxo42^em1(IMPC)J/Fbxo42^em1(IMPC)J C57BL/6NJ-Fbxo42^em1(IMPC)J/Mmjax	abnormal embryo size	J:211773
	abnormal facial morphology	J:211773
	abnormal skin appearance	J:211773
	edema	J:211773
	hemorrhage	J:211773
	preweaning lethality, complete penetrance	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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