Del(5Gtf2i-Fkbp6)1Vcam
Targeted Allele Detail

Summary

• Symbol: Del(5Gtf2i-Fkbp6)1Vcam
• Name: deletion, Chr5, Victoria Campuzano 1; deletion, Chr 5, Victoria Campuzano 1
• MGI ID: MGI:5555958
• Synonyms: CD, ESSP9
• Gene: Del(5Gtf2i-Fkbp6)1Vcam Location: unknown Genetic Position: Chr5, Syntenic

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:216195
• Parent Cell Line: Other (see notes) (ES Cell)
• Strain of Origin: Not Specified

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutations: Insertion, Intergenic deletion, Intragenic deletion
• Del(5Gtf2i-Fkbp6)1Vcam involves 41 genes/genome features (Gm26340, n-R5s178, Gm25315 ...) View all
• Mutation details: Cre mediated recombination between Gtf2i^tm1Vcam and Fkbp6^tm1Vcam deleted the genomic region between the two genes. (J:216195)

Disease models

Expression

In Mice Carrying this Mutation:	1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation:	14 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 0 strains available Cell Lines: 0 lines available
• Carrying any Del(5Gtf2i-Fkbp6)1Vcam Mutation: 0 strains or lines available

Notes

ES cell line = G6

References

• Original: J:216195 Segura-Puimedon M, et al., Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder. Hum Mol Genet. 2014 Dec 15;23(24):6481-94
• All: 8 reference(s)