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Allele : Arhgap35<m1Bchd> Rho GTPase activating protein 35; mutation 1, Maxime Bouchard

Primary Identifier  MGI:5789382 Allele Type  Chemically induced (ENU)
Attribute String  Null/knockout Gene  Arhgap35
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false
molecularNote  ENU mutagenesis induced an A to T nucleotide exchange that alters amino acid leucine 1396 to glutamine in the C-terminal RhoGAP domain. The L1396Q substitution is a loss-of-function mutation that results in decreased GTPase-activating protein (GAP) activity for the prototypical Rho family members, RhoA and Rac1, likely due to disrupted ordering of the Rho binding surface.
  • mutations:
  • Single point mutation
  • synonyms:
  • Arhgap35<D34>,
  • Arhgap35<D34>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

3 Publication categories

Trail: Allele