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Symbol Name ID |
Slc1a3
solute carrier family 1 (glial high affinity glutamate transporter), member 3 MGI:99917 |
| Darker colors indicate more annotations |
| Human Phenotypes | Vertigo |
| Disease(s) Associated with SLC1A3 | |
| episodic ataxia type 6 |
| Mouse Phenotypes | cochlear inner hair cell degeneration |
abnormal auditory brainstem response waveform shape |
increased or absent threshold for auditory brainstem response |
increased susceptibility to noise-induced hearing loss |
increased susceptibility to ototoxicity-induced hearing loss |
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| Availability | Mouse Genotype | |||||
| Slc1a3tm1Kta/Slc1a3tm1Kta | ||||||
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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last database update 04/16/2024 MGI 6.23 |
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