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Rfx4m269Asp
Chemically induced Allele Detail
Summary
Symbol: Rfx4m269Asp
Name: regulatory factor X, 4 (influences HLA class II expression); mutation 269, Andrew S Peterson
MGI ID: MGI:3799278
Synonyms: Rfx4L298P, Rfx4line269
Gene: Rfx4  Location: Chr10:84591926-84742402 bp, + strand  Genetic Position: Chr10, 41.63 cM, cytoband C1
Alliance: Rfx4m269Asp page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced nucleotide transition that resulted in an amino acid substitution of proline for leucine in the C dimerization domain. (J:136795)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 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 Rfx4 Mutation:  48 strains or lines available
References
Original:  J:136795 Zarbalis K, et al., A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical development. PLoS Biol. 2004 Aug;2(8):E219
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