Symbol Name ID |
Msx2
msh homeobox 2 MGI:97169 |
Reference
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J:15514 Jabs EW, Muller U, Li X, Ma L, Luo W, Haworth IS, Klisak I, Sparkes R, Warman ML, Mulliken JB, Snead ML, Maxson R, A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell. 1993 Nov 5;75(3):443-50 |
Age | E15.5 | P |
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 11/12/2024 MGI 6.24 |
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