About   Help   FAQ
Celf4Ff
Transgenic Allele Detail
Summary
Symbol: Celf4Ff
Name: CUGBP, Elav-like family member 4; frequent flyer
MGI ID: MGI:3037035
Synonyms: Ff
Gene: Celf4  Location: Chr18:25610689-25887214 bp, - strand  Genetic Position: Chr18, 13.92 cM, cytoband B1
Alliance: Celf4Ff page
Celf4Ff/Brunol4+ mice exhibit seizures

Show the 1 phenotype image(s) involving this allele.

Transgene
origin
Strain of Origin:  C57BL/6J
Transgene
description
Transgene Type:    Transgenic
Mutation:    Insertion
 
Mutation detailsMultiple copies (>3) of a non-expressing transgene inserted into the first intron of the gene. In total RNA samples from newborn mice, no transcript of the endogenous gene was detected in homozygotes and approximately 45% reduction was seen in heterozygotes. (J:123744)
Phenotypes
Loading...
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Celf4 Mutation:  27 strains or lines available
References
Original:  J:123744 Yang Y, et al., Complex seizure disorder caused by Brunol4 deficiency in mice. PLoS Genet. 2007 Jul 27;3(7):e124
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory