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C20orf32 probe1 Probe Detail
Nucleotide
Probe/Clone
  • Name
    C20orf32 probe1
  • Sequence Type
    Not Specified
  • ID
    MGI:3720462
  • Region Covered
    3' untranslated region
Source
  • Species
    Not Specified
Genes
Cass4 Cas scaffolding protein family member 4
Expression
  • Assay Results
    4
References
J:122749 Lu W, et al., NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects. PLoS Genet. 2007 May 25;3(5):e80
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
10/22/2024
MGI 6.24 		The Jackson Laboratory