Cmya5^tm1Cap
Targeted Allele Detail

Summary

• Symbol: Cmya5^tm1Cap
• Name: cardiomyopathy associated 5; targeted mutation 1, Yassemi Capetanaki
• MGI ID: MGI:7261228
• Gene: Cmya5 Location: Chr13:93177221-93281232 bp, - strand Genetic Position: Chr13, 47.81 cM, cytoband C3
• Alliance: Cmya5^tm1Cap page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:322761
• Parent Cell Line: W4 (ES Cell)
• Strain of Origin: 129S6/SvEvTac

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutations: Insertion, Intragenic deletion
• The targeting construct replaced a portion of the second exon with a neomycin resistance cassette. (J:322761)

Expression

In Structures Affected by this Mutation:

8 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 Cmya5 Mutation: 148 strains or lines available

References

• Original: J:322761 Tsoupri E, et al., Myospryn deficiency leads to impaired cardiac structure and function and schizophrenia-associated symptoms. Cell Tissue Res. 2021 May 26
• All: 1 reference(s)