Gene Expression Literature Detail
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Symbol Name ID |
Slc1a3
solute carrier family 1 (glial high affinity glutamate transporter), member 3 MGI:99917 |
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Reference
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J:266183 Cerrato V, Mercurio S, Leto K, Fuca E, Hoxha E, Bottes S, Pagin M, Milanese M, Ngan CY, Concina G, Ottolenghi S, Wei CL, Bonanno G, Pavesi G, Tempia F, Buffo A, Nicolis SK, Sox2 conditional mutation in mouse causes ataxic symptoms, cerebellar vermis hypoplasia, and postnatal defects of Bergmann glia. Glia. 2018 Sep;66(9):1929-1946 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | P |
| Immunohistochemistry (section) | |
| In situ RNA (section) | |
| Immunohistochemistry (whole mount) | |
| In situ RNA (whole mount) | |
| In situ reporter (knock in) | |
| Northern blot | |
| Western blot | |
| RT-PCR | |
| cDNA clones | |
| RNase protection | |
| Nuclease S1 | |
| Primer Extension |
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 12/10/2024 MGI 6.24 |
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