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Symbol
Name
ID
Whrn
whirlin
MGI:2682003
Phenotype annotations related to hearing/vestibular/ear
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Abnormal vestibular function
Absent vestibular function
Sensorineural hearing impairment
Hearing impairment
Disease(s) Associated with WHRN
autosomal recessive nonsyndromic deafness 31
Usher syndrome type 2D

Mouse Phenotypes
hearing/vestibular/ear phenotype
decreased cochlear hair cell number
abnormal cochlear hair cell stereociliary bundle morphology
abnormal cochlear hair bundle transient lateral links morphology
short inner hair cell stereocilia
abnormal outer hair cell stereociliary bundle morphology
short outer hair cell stereocilia
decreased outer hair cell stereocilia number
short cochlear hair cell stereocilia
abnormal cochlear inner hair cell morphology
cochlear inner hair cell degeneration
abnormal cochlear outer hair cell morphology
cochlear outer hair cell degeneration
cochlear hair cell degeneration
abnormal vestibular hair cell stereociliary bundle morphology
short vestibular hair cell stereocilia
abnormal cochlear outer hair cell physiology
absent cochlear microphonics
increased or absent threshold for auditory brainstem response
abnormal auditory summating potential
abnormal cochlear frequency tuning
absent cochlear nerve compound action potential
abnormal distortion product otoacoustic emission
absent distortion product otoacoustic emissions
impaired hearing
deafness
Availability Mouse Genotype
Whrnhb/Whrnhb
Whrntm1a(EUCOMM)Wtsi/Whrntm1a(EUCOMM)Wtsi
Whrntm1b(EUCOMM)Wtsi/Whrntm1b(EUCOMM)Wtsi *
Whrntm1Tili/Whrntm1Tili
Whrnwi/Whrnwi
Whrnwi/Whrn+

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
04/09/2024
MGI 6.23
The Jackson Laboratory