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Arhgap31 probe Probe Detail
Nucleotide
Probe/Clone
  • Name
    Arhgap31 probe
  • Sequence Type
    genomic
  • ID
    MGI:5301564
  • Region Covered
    3' untranslated region
  • Amplification
    Primers
  • Insert Size
    0.543kb
  • Note
    This probe was generated by PCR using primers MGI:5301568.
Source
  • Species
    mouse, laboratory
Genes
Arhgap31 Rho GTPase activating protein 31
Expression
  • Assay Results
    17
References
J:177944 Southgate L, et al., Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies. Am J Hum Genet. 2011 May 13;88(5):574-85

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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last database update
03/25/2025
MGI 6.24
The Jackson Laboratory