About   Help   FAQ
Vav1m2Btlr
Chemically induced Allele Detail
Summary
Symbol: Vav1m2Btlr
Name: vav 1 oncogene; mutation 2, Bruce Beutler
MGI ID: MGI:6199674
Synonyms: plain_sight
Gene: Vav1  Location: Chr17:57586100-57635031 bp, + strand  Genetic Position: Chr17, 29.76 cM
Alliance: Vav1m2Btlr page
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Beutler Mutagenetix
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsENU-induced G to A transition at base pair 57,297,122 (v38) on chromosome 17, or base pair 18,044 in the GenBank genomic region NC_000083. The mutation corresponds to residue 621 in the mRNA sequence NM_011691 within exon 5 of 27 total exons. The mutation results in a glutamic acid to lysine substitution at amino acid 175 (E175K) in the VAV1 protein. (J:265130)
Inheritance:    Recessive
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
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 Vav1 Mutation:  60 strains or lines available
References
Original:  J:265130 Zhong X, et al., Mutagenetix entry for plain_sight. MGI Direct Data Submission. 2018;
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory