Summary | Transgene origin | Transgene description | Expression | Phenotypes | Find Mice (IMSR) | References

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.

Strain of Origin:

C57BL/6J

Transgene Type:    Transgenic Mutation:    Insertion   Mutation details: Multiple 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)

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

1 anatomical structure(s)

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

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)