Symbol Name ID

Smad9 SMAD family member 9 MGI:1859993

Reference

J:166923 Wang B, Sinha T, Jiao K, Serra R, Wang J, Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B. Hum Mol Genet. 2011 Jan 15;20(2):271-85

Detailed expression data for these assays: 4 results

Indicates gene expression was analyzed but not necessarily detected.

Age	E11.5
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

Comments: The antibody used to obtain this data recognizes the phosphorylated form of the protein. Age of embryo at noon of plug day not specified in reference.