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

Symbol:	Celf4tm1.1Frk
Name:	CUGBP, Elav-like family member 4; targeted mutation 1.1, Wayne N Frankel
MGI ID:	MGI:5425629
Synonyms:	Celf4flox
Gene:	Celf4  Location: Chr18:25610689-25887214 bp, - strand  Genetic Position: Chr18, 13.92 cM, cytoband B1
Alliance:	Celf4tm1.1Frk page

Germline Transmission:	Earliest citation of germline transmission: J:181678
Parent Cell Line:	R1 (ES Cell)
Strain of Origin:	(129X1/SvJ x 129S1/Sv)F1-Kitl+

Allele Type:    Targeted (Conditional ready, No functional change) Mutation:    Insertion   Mutation details: LoxP sites were inserted 2.1 kb upstream and 444bp downstream of exon 1. An frt-flanked neo selection cassette was deleted from intron 1 in the final allele. (J:181678)

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

In Mice Carrying this Mutation:

1 RNA-Seq or microarray experiment(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Celf4 Mutation:	27 strains or lines available

Original:	J:181678 Wagnon JL, et al., Etiology of a genetically complex seizure disorder in Celf4 mutant mice. Genes Brain Behav. 2011 Oct;10(7):765-77
All:	5 reference(s)