Rpgrip1^mpc269H
Chemically induced Allele Detail

Summary

• Symbol: Rpgrip1^mpc269H
• Name: retinitis pigmentosa GTPase regulator interacting protein 1; muta-ped-c3pde 269, Harwell
• MGI ID: MGI:5792096
• Gene: Rpgrip1 Location: Chr14:52348161-52401003 bp, + strand Genetic Position: Chr14, 26.81 cM
• Alliance: Rpgrip1^mpc269H page

Mutation origin

• Strain of Origin: C57BL/6J
• Project Collection: Harwell ENU Mutagenesis

Mutation description

• Allele Type: Chemically induced (ENU) (Not Specified)
• Mutation: Not Specified
• ENU mutagenesis induced an intronic mutation. (J:234901)
• Inheritance: Recessive

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 Rpgrip1 Mutation: 70 strains or lines available

References

• Original: J:234901 Potter PK, et al., Novel gene function revealed by mouse mutagenesis screens for models of age-related disease. Nat Commun. 2016;7:12444
• All: 1 reference(s)