Del(7Chrna7-Fan1)3Arte
Targeted Allele Detail

Summary

• Symbol: Del(7Chrna7-Fan1)3Arte
• Name: deletion, Chr 7, TaconicArtemis
• MGI ID: MGI:6150456
• Synonyms: Del3Arte, Df(h15q13)
• Gene: Del(7Chrna7-Fan1)3Arte Location: unknown Genetic Position: Chr7, Syntenic

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:260165
• Parent Cell Line: Not Specified (ES Cell)
• Strain of Origin: C57BL/6NTac

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutations: Intergenic deletion, Intragenic deletion
• Del(7Chrna7-Fan1)3Arte involves 30 genes/genome features (Gm32902, Gm22228, Gm45987 ...) View all
• Mutation details: A loxP site was inserted upstream of Chrna7 and downstream of Fan1. Cre-mediated recombination deleted the 1.28 Mb intervening sequence. (J:260165)

Disease models

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: 0 strains available Cell Lines: 0 lines available
• Carrying any Del(7Chrna7-Fan1)3Arte Mutation: 0 strains or lines available

References

• Original: J:260165 Fejgin K, et al., A mouse model that recapitulates cardinal features of the 15q13.3 microdeletion syndrome including schizophrenia- and epilepsy-related alterations. Biol Psychiatry. 2014 Jul 15;76(2):128-37
• All: 5 reference(s)