Gene Expression Literature Detail
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Symbol Name ID |
Slc26a4
solute carrier family 26, member 4 MGI:1346029 |
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Reference
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J:285979 Kim MA, Kim SH, Ryu N, Ma JH, Kim YR, Jung J, Hsu CJ, Choi JY, Lee KY, Wangemann P, Bok J, Kim UK, Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing. Theranostics. 2019;9(24):7184-7199 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E13.5 | E14.5 | E16.5 | P |
| Immunohistochemistry (section) | |
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| In situ RNA (section) | ||||
| Immunohistochemistry (whole mount) | ||||
| In situ RNA (whole mount) | ||||
| In situ reporter (knock in) | ||||
| Northern blot | ||||
| Western blot | ||||
| RT-PCR | |
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| 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 11/12/2024 MGI 6.24 |
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