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Symbol
Name
ID

Wbp2
WW domain binding protein 2
MGI:104709

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	Hearing impairment
Disease(s) Associated with WBP2	Hearing impairment
autosomal recessive nonsyndromic deafness 107

Mouse Phenotypes		hearing/vestibular/ear phenotype	abnormal cochlear IHC afferent innervation pattern	abnormal cochlear OHC afferent innervation pattern	abnormal organ of Corti morphology	abnormal auditory brainstem response waveform shape	increased or absent threshold for auditory brainstem response	abnormal auditory summating potential	abnormal distortion product otoacoustic emission	sensorineural hearing loss
Availability	Mouse Genotype
	Wbp2^{tm2a(EUCOMM)Wtsi}/Wbp2^{tm2a(EUCOMM)Wtsi}	*

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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