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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Plscr5
phospholipid scramblase family, member 5
MGI:3779462
10 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Plscr5em1(IMPC)J/Plscr5em1(IMPC)J
C57BL/6NJ-Plscr5em1(IMPC)J/Mmjax 		abnormal auditory brainstem response J:211773
decreased startle reflex J:211773
Plscr5em1Wagq/Plscr5+
involves: C57BL/6 		cochlear outer hair cell degeneration J:368539
impaired hearing J:368539
Plscr5em1Wagq/Plscr5em1Wagq
involves: C57BL/6 		abnormal cochlear hair cell physiology J:368539
cochlear outer hair cell degeneration J:368539
decreased auditory brainstem response wave amplitude J:368539
decreased inner hair cell stereocilia number J:368539
decreased outer hair cell stereocilia number J:368539
normal hearing/vestibular/ear phenotype J:368539
impaired hearing J:368539
increased or absent distortion product otoacoustic emission threshold J:368539
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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Send questions and comments to User Support. 		last database update
09/30/2025
MGI 6.24 		The Jackson Laboratory