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pMGli20 Probe Detail
Nucleotide
Probe/Clone
  • Name
    pMGli20
  • Sequence Type
    cDNA
  • ID
    MGI:17399
  • Region Covered
    3' portion of coding region
  • Insert Size
    ~1.2kb
Source
  • Species
    mouse, laboratory
  • Age
    embryonic day 8.5
  • Tissue
    embryo
Genes
Gli3 GLI-Kruppel family member GLI3
Polymorphisms
J:28830 Brunialti AL, et al., Genomics. 1995 Sep 1;29(1):131-5
Endonuclease Gene Allele Fragments Strains
BglII Gli3 b 5.1kb C57BL/6
s 4.8kb SEG/Pas, STF/Pas
References
J:1718 Vortkamp A, et al., Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt). Mamm Genome. 1992;3(8):461-3
J:28830 Brunialti AL, et al., The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13. Genomics. 1995 Sep 1;29(1):131-5
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
05/21/2024
MGI 6.23 		The Jackson Laboratory