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Vangl2M1Yzcm
Chemically induced Allele Detail
Summary
Symbol: Vangl2M1Yzcm
Name: VANGL planar cell polarity 2; mutation 1, Yangzhou University Comparative Medicine Center
MGI ID: MGI:5468724
Gene: Vangl2  Location: Chr1:171828527-171856011 bp, - strand  Genetic Position: Chr1, 79.54 cM
Alliance: Vangl2M1Yzcm page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU induced a C/T transition mutation that resulted in substitution of a glutamine codon (Q) for a stop (nonsense) codon at position 449. (J:193593)
Inheritance:    Dominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 1 assay results
In Structures Affected by this Mutation: 3 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:193593 Chen B, et al., Loop-tail phenotype in heterozygous mice and neural tube defects in homozygous mice result from a nonsense mutation in the Vangl2 gene. Genet Mol Res. 2013 Jan 22;12(AOP)
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
04/23/2024
MGI 6.23
The Jackson Laboratory