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Vangl2ska17
Chemically induced Allele Detail
Summary
Symbol: Vangl2ska17
Name: VANGL planar cell polarity 2; skeletal/axial 17
MGI ID: MGI:3038827
Synonyms: Lpm2Jus, skam17Jus, Vangl2R259L
Gene: Vangl2  Location: Chr1:171828527-171856011 bp, - strand  Genetic Position: Chr1, 79.54 cM
Alliance: Vangl2ska17 page
Mutation
origin
Strain of Origin:  C57BL/6Brd-Tyrc-Brd
Project Collection: Mutagenesis for Dev. Defects
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsA missense mutation that alters a G to a T at position 776 in the cDNA which changes arginine 259 to leucine was induced by ENU treatment. Western blot analysis indicated protein levels in the brains of homozygous mice at E16.5 were about 90% that of wild-type littermates. (J:169664)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 3 assay results
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: 0 strains available      Cell Lines: 0 lines available
Carrying any Vangl2 Mutation:  34 strains or lines available
References
Original:  J:89098 The Mouse Genome Project at The Baylor College of Medicine, Heritable mouse mutants from the Mouse Mutagenesis for Developmental Defects Program. MGI Direct Data Submission. 2004-5;
All:  2 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
12/10/2024
MGI 6.24
The Jackson Laboratory