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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 |
| Mouse Phenotypes | nervous system phenotype |
increased susceptibility to pharmacologically induced seizures |
seizures |
abnormal kindling response |
cochlear inner hair cell degeneration |
abnormal Purkinje cell morphology |
decreased retina ganglion cell number |
abnormal optic nerve morphology |
optic nerve cupping |
optic nerve degeneration |
abnormal nervous system physiology |
abnormal excitatory postsynaptic currents |
prolonged excitatory postsynaptic current decay time |
short excitatory postsynaptic current rise time |
abnormal synaptic glutamate release |
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| Availability | Mouse Genotype | |||||||||||||||
| Slc1a3tm1Kta/Slc1a3tm1Kta | * | |||||||||||||||
| Slc1a3tm1Wst/Slc1a3tm1Wst | ||||||||||||||||
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 07/02/2024 MGI 6.13 |
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