About Help FAQ

Symbol
Name
ID

Slc17a8
solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8
MGI:3039629

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	Sensorineural hearing impairment
Disease(s) Associated with SLC17A8	Abnormal vestibular function	Sensorineural hearing impairment
autosomal dominant nonsyndromic deafness 25

Mouse Phenotypes		hearing/vestibular/ear phenotype	decreased cochlear inner hair cell number	abnormal cochlear IHC efferent innervation pattern	abnormal inner hair cell synaptic ribbon morphology	abnormal cochlear inner hair cell physiology	abnormal auditory brainstem response	increased or absent threshold for auditory brainstem response	absent cochlear nerve compound action potential	deafness	sensorineural hearing loss
Availability	Mouse Genotype	hearing/vestibular/ear phenotype	decreased cochlear inner hair cell number	abnormal cochlear IHC efferent innervation pattern	abnormal inner hair cell synaptic ribbon morphology	abnormal cochlear inner hair cell physiology	abnormal auditory brainstem response		absent cochlear nerve compound action potential	deafness	sensorineural hearing loss
	Slc17a8^em1(IMPC)Mbp/Slc17a8^em1(IMPC)Mbp
	Slc17a8^tm1Edw/Slc17a8^tm1Edw
	Slc17a8^tm1Selm/Slc17a8^tm1Selm	*

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23