Gene Expression Literature Detail
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Symbol Name ID |
Fgf17
fibroblast growth factor 17 MGI:1202401 |
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Reference
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J:157828 Lancioni A, Pizzo M, Fontanella B, Ferrentino R, Napolitano LM, De Leonibus E, Meroni G, Lack of Mid1, the mouse ortholog of the Opitz syndrome gene, causes abnormal development of the anterior cerebellar vermis. J Neurosci. 2010 Feb 24;30(8):2880-7 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E13.5 | E14.5 |
| Immunohistochemistry (section) | ||
| In situ RNA (section) | |
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| 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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