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Allele : Arhgef9<tm1.1Betz> CDC42 guanine nucleotide exchange factor 9; targeted mutation 1.1, Heinrich Betz

Primary Identifier  MGI:3757650 Allele Type  Targeted
Attribute String  Null/knockout Gene  Arhgef9
Transmission  Germline Strain of Origin  129P2/OlaHsd
Is Recombinase  false Is Wild Type  false
molecularNote  Transfection of ES cells with a cre construct was used to remove exon 5 along with an inserted neo cassette. Exon 5 encodes part of the catalytic RhoGEF domain. Its deletion and resulting frameshift are predicted to destroy the function of the protein and eliminate the entire C-terminus. The absence of full length and truncated protein products was confirmed by western blot on brain homogenates using either a monoclonal specific for the N-terminus or polyclonal antibody against Arhgef9.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • Collybistin knock-out,
  • Collybistin knock-out
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

7 Publication categories