Gene Expression Literature Detail
|
Symbol Name ID |
Spp1
secreted phosphoprotein 1 MGI:98389 |
|
Reference
|
J:283626 Yin L, Du X, Li C, Xu X, Chen Z, Su N, Zhao L, Qi H, Li F, Xue J, Yang J, Jin M, Deng C, Chen L, A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis. Bone. 2008 Apr;42(4):631-43 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E16.5 | E17.5 |
| 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) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 12/30/2025 MGI 6.24 |
|
|
|
||
Analysis Tools