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Symbol
Name
ID

Slc19a2
solute carrier family 19 (thiamine transporter), member 2
MGI:1928761

Phenotype annotations related to hearing/vestibular/ear

Darker colors indicate more annotations

Human Phenotypes	Sensorineural hearing impairment
Disease(s) Associated with SLC19A2	Sensorineural hearing impairment
thiamine-responsive megaloblastic anemia syndrome

Mouse Phenotypes		cochlear inner hair cell degeneration	cochlear outer hair cell degeneration	increased or absent threshold for auditory brainstem response	abnormal distortion product otoacoustic emission	impaired hearing	sensorineural hearing loss
Availability	Mouse Genotype	cochlear inner hair cell degeneration	cochlear outer hair cell degeneration		abnormal distortion product otoacoustic emission	impaired hearing	sensorineural hearing loss
	Slc19a2^tm1Ejn/Slc19a2^tm1Ejn
	Slc19a2^tm1Gelb/Slc19a2^tm1Gelb

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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