Gene Expression Literature Detail
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Symbol Name ID |
Th
tyrosine hydroxylase MGI:98735 |
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Reference
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J:137167 Tennese AA, Gee CB, Wevrick R, Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons. Dev Dyn. 2008 Jul;237(7):1935-43 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E11.5 | E12.5 | E14.5 | E16.5 | E18.5 |
| Immunohistochemistry (section) | |
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| In situ RNA (section) | |||||
| Immunohistochemistry (whole mount) | |
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| 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 09/30/2025 MGI 6.24 |
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