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pSPORT-beta-spectrin2 Probe Detail
Nucleotide
Probe/Clone
  • Name
    pSPORT-beta-spectrin2
  • Sequence Type
    cDNA
  • ID
    MGI:2178451
  • Region Covered
    6412-8172bp
Source
  • Species
    Not Specified
Genes
Sptbn1 spectrin beta, non-erythrocytic 1
Expression
  • Assay Results
    3
References
J:75954 Dunwoodie SL, et al., Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm. Development. 2002 Apr;129(7):1795-806
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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Funding Information
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Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory