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Msx2-pS, Msx2-pT Primer Detail
Primers
  • Name
    Msx2-pS, Msx2-pT
  • Primer 1 Sequence
    ATACAGGAGCCCGGCAGATACT
  • Primer 2 Sequence
    TCCGGTTGGTCTTGTGTTTCC
  • ID
    MGI:5754787
Genes
Msx2 msh homeobox 2
Expression
  • Assay Results
    2
References
J:166923 Wang B, et al., 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
Contributing Projects:
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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Send questions and comments to User Support. 		last database update
01/20/2026
MGI 6.24 		The Jackson Laboratory