Clrn2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Clrn2
clarin 2
MGI:3646230

18 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Clrn2^em1(IMPC)J/Clrn2^em1(IMPC)J C57BL/6NJ-Clrn2^em1(IMPC)J/Mmjax	abnormal auditory brainstem response	J:211773
	abnormal startle reflex	J:211773
	decreased bone mineral content	J:211773
	decreased bone mineral density	J:211773
	decreased lean body mass	J:211773
	decreased prepulse inhibition	J:211773
	decreased startle reflex	J:211773
	increased total body fat amount	J:211773
	increased vertical activity	J:211773
Clrn2^em1H/Clrn2^mpc169H involves: C57BL/6J	increased or absent threshold for auditory brainstem response	J:283627
Clrn2^mpc169H/Clrn2^mpc169H C57BL/6J-Clrn2^mpc169H	abnormal cochlear inner hair cell physiology	J:283627
	abnormal distortion product otoacoustic emission	J:283627
	abnormal hair cell mechanoelectric transduction	J:283627
	deafness	J:283627
	normal hearing/vestibular/ear phenotype	J:283627
	increased or absent threshold for auditory brainstem response	J:283627
	nonsyndromic hearing loss	J:283627
	normal vision/eye phenotype	J:283627
Clrn2^mpc169H/Clrn2^mpc169H involves: BALB/c * C3H/HeH * C57BL/6J	abnormal inner ear vestibule morphology	J:234901
	deafness	J:234901

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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