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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
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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: 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)
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last database update
10/22/2024
MGI 6.24
The Jackson Laboratory