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Plxna2nmf454
Chemically induced Allele Detail
Summary
Symbol: Plxna2nmf454
Name: plexin A2; neuroscience mutagenesis facility 454
MGI ID: MGI:3793765
Synonyms: NMF454
Gene: Plxna2  Location: Chr1:194302020-194499177 bp, + strand  Genetic Position: Chr1, 98.27 cM, cytoband H6
Alliance: Plxna2nmf454 page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Nucleotide substitutions
 
Mutation detailsENU mutagenesis was used to induce a nucleotide substitution that resulted in an amino acid substitution of glutamic acid for alanine at position 396 (A396E). This amino acid is involved in Sema6a binding to plexin-A2. (J:135408)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Plxna2 Mutation:  127 strains or lines available
References
Original:  J:135408 Renaud J, et al., Plexin-A2 and its ligand, Sema6A, control nucleus-centrosome coupling in migrating granule cells. Nat Neurosci. 2008 Apr;11(4):440-9
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
04/16/2024
MGI 6.23
The Jackson Laboratory