About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Fbxo2
F-box protein 2
MGI:2446216
17 phenotypes from 2 alleles in 2 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Fbxo2tm1b(EUCOMM)Wtsi/Fbxo2tm1b(EUCOMM)Wtsi
C57BL/6N-Fbxo2tm1b(EUCOMM)Wtsi/Nju 		decreased fasting circulating glucose level J:211773
decreased locomotor activity J:211773
decreased startle reflex J:211773
increased circulating glucose level J:211773
Fbxo2tm1Hlp/Fbxo2tm1Hlp
B6.129-Fbxo2tm1Hlp 		abnormal auditory brainstem response waveform shape J:121568
abnormal Claudius cell morphology J:121568
abnormal cochlear hair cell morphology J:121568
abnormal organ of Corti supporting cell morphology J:121568
normal behavior/neurological phenotype J:121568
cochlear degeneration J:121568
cochlear ganglion degeneration J:121568
cochlear hair cell degeneration J:121568
deafness J:121568
degeneration of organ of Corti supporting cells J:121568
increased or absent threshold for auditory brainstem response J:121568
increased susceptibility to age-related hearing loss J:121568
normal nervous system phenotype J:121568
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory