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Cad probe Probe Detail
Nucleotide
Probe/Clone
  • Name
    Cad probe
  • Sequence Type
    genomic
  • ID
    MGI:5441722
  • Region Covered
    3' untranslated region and the coding sequence
  • Insert Size
    0.302kb
  • Note
    This DNA was generated by PCR using primers MGI:5441614.
Source
  • Species
    mouse, laboratory
Genes
Cad carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase
Expression
  • Assay Results
    12
References
J:187427 Rainger J, et al., Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH. Hum Mol Genet. 2012 Sep 15;21(18):3969-83
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
04/16/2024
MGI 6.23 		The Jackson Laboratory