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Symbol Name ID |
Slc1a3
solute carrier family 1 (glial high affinity glutamate transporter), member 3 MGI:99917 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Nystagmus |
Hypometric saccades |
Diplopia |
Photophobia |
| Disease(s) Associated with SLC1A3 | ||||
| episodic ataxia type 6 |
| Mouse Phenotypes | vision/eye phenotype |
decreased retina ganglion cell number |
abnormal optic nerve morphology |
optic nerve cupping |
optic nerve degeneration |
abnormal retina ganglion layer morphology |
abnormal retina inner nuclear layer morphology |
retina degeneration |
abnormal electroretinogram waveform feature |
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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 04/30/2024 MGI 6.23 |
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