Symbol
Name
ID

Slc26a4
solute carrier family 26, member 4
MGI:1346029

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Ataxia	Abnormality of speech or vocalization	Intellectual disability
Disease(s) Associated with SLC26A4
Pendred Syndrome

Mouse Phenotypes

decreased cochlear hair cell number

absent cochlear hair cells

abnormal cochlear hair cell stereociliary bundle morphology

fused inner hair cell stereocilia

cochlear inner hair cell degeneration

cochlear outer hair cell degeneration

cochlear hair cell degeneration

abnormal hair cell morphology

decreased vestibular hair cell number

vestibular hair cell degeneration

absent cochlear ganglion

Availability

Mouse Genotype

Slc26a4^em1Jgao/Slc26a4^em1Jgao

Slc26a4^loop/Slc26a4^loop

Slc26a4^pdsm/Slc26a4^pdsm

Slc26a4^tm1.1Dontu/Slc26a4^tm1.1Dontu

Slc26a4^tm1Egr/Slc26a4^tm1Egr

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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