Fbxo41 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fbxo41
F-box protein 41
MGI:1261912

24 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fbxo41^{tm1(KOMP)Vlcg}/Fbxo41^{tm1(KOMP)Vlcg} involves: C57BL/6NTac	abnormal cerebellar molecular layer	J:222558
	abnormal cerebellum external granule cell layer morphology	J:222558
	abnormal gait	J:222558
	abnormal neuronal migration	J:222558
	ataxia	J:222558
	decreased body weight	J:222558
	decreased brain weight	J:222558
	impaired balance	J:222558
	impaired coordination	J:222558
	limb grasping	J:222558
	normal nervous system phenotype	J:222558
	postnatal growth retardation	J:222558
	postnatal lethality, incomplete penetrance	J:222558
	premature death	J:222558
	small cerebellum	J:222558
	tremors	J:222558
Fbxo41^{tm1.1(KOMP)Vlcg}/Fbxo41^{tm1.1(KOMP)Vlcg} C57BL/6N-Fbxo41^{tm1.1(KOMP)Vlcg}/Ucd	abnormal auditory brainstem response	J:211773
	decreased circulating cholesterol level	J:211773
	decreased grip strength	J:211773
	eye hemorrhage	J:211773
	hyperactivity	J:211773
	increased heart weight	J:211773
	increased kidney weight	J:211773
	increased startle reflex	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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