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Phox2b probe6 Probe Detail
Nucleotide
Probe/Clone
  • Name
    Phox2b probe6
  • Sequence Type
    Not Specified
  • ID
    MGI:5582618
Source
  • Species
    Not Specified
Genes
Phox2b paired-like homeobox 2b
Expression
  • Assay Results
    2
References
J:137167 Tennese AA, et al., Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons. Dev Dyn. 2008 Jul;237(7):1935-43
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
03/25/2025
MGI 6.24 		The Jackson Laboratory