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Symbol Name ID |
Fgf10
fibroblast growth factor 10 MGI:1099809 |
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Reference
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J:72517 Hajihosseini MK, Wilson S, De Moerlooze L, Dickson C, A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes. Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):3855-60 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E18 |
| 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 09/30/2025 MGI 6.24 |
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