Cabp5^tm1Fha
Targeted Allele Detail

Summary

• Symbol: Cabp5^tm1Fha
• Name: calcium binding protein 5; targeted mutation 1, Francoise Haeseleer
• MGI ID: MGI:6369037
• Gene: Cabp5 Location: Chr7:13132057-13142812 bp, + strand Genetic Position: Chr7, 7.87 cM, cytoband A2
• Alliance: Cabp5^tm1Fha page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:141902
• Parent Cell Line: Not Specified (ES Cell)
• Strain of Origin: 129

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutations: Insertion, Intragenic deletion
• Mutation details: A neomycin resistance cassette replaced exon 1 and 2. Western blot analysis confirmed the absence of protein expression in the retina. (J:141902)

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 Cabp5 Mutation: 15 strains or lines available

References

• Original: J:141902 Rieke F, et al., Characterization of Ca2+-binding protein 5 knockout mouse retina. Invest Ophthalmol Vis Sci. 2008 Nov;49(11):5126-35
• All: 1 reference(s)