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Arhgap35em1Slp
Endonuclease-mediated Allele Detail
Summary
Symbol: Arhgap35em1Slp
Name: Rho GTPase activating protein 35; endonuclease-mediated mutation 1, Samuel L Pfaff
MGI ID: MGI:7621681
Synonyms: p190R1284A
Gene: Arhgap35  Location: Chr7:16228398-16349313 bp, - strand  Genetic Position: Chr7, 9.15 cM
Alliance: Arhgap35em1Slp page
Mutation
origin
Strain of Origin:  (C57BL/6 x DBA/2)F1
Mutation
description
Allele Type:    Endonuclease-mediated (Not Applicable)
Mutation:    Nucleotide substitutions
 
Mutation detailsArginine codon 1284 (CGG) in exon 4 was changed to alanine (GCA) (p.R1284A) using an sgRNA (equivalent to AAGCACTGAAGGCATCTACC) and an ssODN template with CRISPR/Cas9 technology. The mutation abolishes the GTPase-activating catalytic function of the encoded peptide. (J:276248)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Arhgap35 Mutation:  70 strains or lines available
References
Original:  J:276248 Bonanomi D, et al., p190RhoGAP Filters Competing Signals to Resolve Axon Guidance Conflicts. Neuron. 2019 May 8;102(3):602-620.e9
All:  1 reference(s)

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
03/18/2025
MGI 6.24
The Jackson Laboratory