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Symbol
Name
ID

Sox2
SRY (sex determining region Y)-box 2
MGI:98364

Phenotype annotations related to hearing/vestibular/ear

Darker colors indicate more annotations

Human Phenotypes	Sensorineural hearing impairment	Bilateral sensorineural hearing impairment	Hearing impairment
Disease(s) Associated with SOX2
syndromic microphthalmia 3

Mouse Phenotypes		abnormal inner ear morphology	dilated cochlea	abnormal cochlear hair cell morphology	decreased cochlea coiling	absent vestibular hair cells	abnormal semicircular canal morphology	abnormal vestibular saccule morphology	abnormal sulcus ampullaris morphology	decreased cochlear nerve compound action potential	deafness
Availability	Mouse Genotype	abnormal inner ear morphology	dilated cochlea	abnormal cochlear hair cell morphology	decreased cochlea coiling	absent vestibular hair cells	abnormal semicircular canal morphology	abnormal vestibular saccule morphology	abnormal sulcus ampullaris morphology	decreased cochlear nerve compound action potential	deafness
	Sox2^ysb/Sox2^ysb
	Sox2^tm1Rlb/Sox2^ysb

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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