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Symbol
Name
ID
Clrn1
clarin 1
MGI:2388124
Phenotype annotations related to nervous system
Darker colors indicate more annotations

Mouse Phenotypes
abnormal synaptic vesicle exocytosis
absent cochlear inner hair cells
absent cochlear outer hair cells
abnormal cochlear hair cell stereociliary bundle morphology
abnormal inner hair cell stereociliary bundle morphology
abnormal orientation of outer hair cell stereociliary bundles
abnormal outer hair cell stereociliary bundle morphology
abnormal cochlear IHC afferent innervation pattern
cochlear inner hair cell degeneration
cochlear outer hair cell degeneration
abnormal cochlear hair cell physiology
abnormal cochlear inner hair cell physiology
decreased cochlear microphonics
abnormal vestibular hair cell physiology
abnormal cochlear nerve compound action potential
abnormal cochlear nerve fiber response
abnormal synapse morphology
abnormal ribbon synapse morphology
cochlear ganglion degeneration
abnormal cochlear nerve morphology
Availability Mouse Genotype
Clrn1tm1.1Kuna/Clrn1tm1.1Kuna
Clrn1tm1.1Kuna/Clrn1tm1.1Kuna
Tg(Atoh1-Clrn1)#Kuna/0
Clrn1tm1.2Ugpa/Clrn1tm1.2Ugpa
Clrn1tm2.1Kuna/Clrn1tm2.1Kuna
Clrn1tm1.1Ugpa/Clrn1tm1.1Ugpa
Myo15atm1.1(cre)Ugds/Myo15a+  (conditional)

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory