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Foxp2R552H
Chemically induced Allele Detail
Summary
Symbol: Foxp2R552H
Name: forkhead box P2; Arg552His
MGI ID: MGI:3793742
Synonyms: Foxp2-R552H
Gene: Foxp2  Location: Chr6:14901348-15441976 bp, + strand  Genetic Position: Chr6, 6.49 cM, cytoband A2
Alliance: Foxp2R552H page
Mutation
origin
Strain of Origin:  (C3H/HeH x BALB/c)F1
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Nucleotide substitutions
 
Mutation detailsENU mutagenesis generated a nucleotide substitution that resulted in an amino acid substitution of histidine for arginine at position 552 (R552H). This mutation is predicted to disrupt the DNA binding and transactivation properties of the protein. (J:135404)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 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 Foxp2 Mutation:  52 strains or lines available
References
Original:  J:93069 Quwailid MM, et al., A gene-driven ENU-based approach to generating an allelic series in any gene. Mamm Genome. 2004 Aug;15(8):585-91
All:  10 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