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

Symbol:	Del(5Gtf2i-Limk1)1Uta
Name:	deletion, Chr 5, Uta Francke 1
MGI ID:	MGI:5317120
Synonyms:	Del1Uta, PD
Gene:	Del(5Gtf2i-Limk1)1Uta  Location: Chr5:134266688-134717452 bp  Genetic Position: Chr5, Syntenic

Germline Transmission:	Earliest citation of germline transmission: J:182796
Parent Cell Line:	AB2.2 (ES Cell)
Strain of Origin:	129S7/SvEvBrd-Hprt1b-m2

Allele Type:    Targeted (Null/knockout) Mutations:    Intergenic deletion, Intragenic deletion   Del(5Gtf2i-Limk1)1Uta involves 15 genes/genome features (Gm26340, n-R5s178, Gtf2i ...) View all   Mutation details: Cre-mediated recombination of mice carrying Gtf2itm1Uta and Limk1tm2Uta removed all genomic sequence between the two alleles (including Gtf2i, Gtf2ird1, Clip2, Syna, Rfc2 Lat2, Eif4h and Limk1). (J:182796)

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

In Structures Affected by this Mutation:

2 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 Del(5Gtf2i-Limk1)1Uta Mutation:	1 strain or line available

Original:	J:182796 Li HH, et al., Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice. EMBO Mol Med. 2009 Apr;1(1):50-65
All:	5 reference(s)