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Symbol
Name
ID

Slc12a7
solute carrier family 12, member 7
MGI:1342283

Phenotype annotations related to hearing/vestibular/ear

Darker colors indicate more annotations

Mouse Phenotypes		abnormal inner ear morphology	absent cochlear outer hair cells	cochlear outer hair cell degeneration	absent organ of Corti	organ of Corti degeneration	increased or absent threshold for auditory brainstem response	impaired hearing	deafness
Availability	Mouse Genotype	abnormal inner ear morphology	absent cochlear outer hair cells	cochlear outer hair cell degeneration	absent organ of Corti	organ of Corti degeneration		impaired hearing	deafness
	Slc12a7^mpc264H/Slc12a7^mpc264H
	Slc12a7^tm1Tjj/Slc12a7^tm1Tjj

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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