Oca2^p-4THO-II
Radiation induced Allele Detail

Summary

• Symbol: Oca2^p-4THO-II
• Name: oculocutaneous albinism II; pink-eyed dilution 4THO-II
• MGI ID: MGI:2673989
• Synonyms: Oca2^p-95R, p^4THO-II
• Gene: Oca2 Location: Chr7:55889508-56186266 bp, + strand Genetic Position: Chr7, 33.44 cM
• Alliance: Oca2^p-4THO-II page

Mutation origin

• Strain of Origin: (C3H/Rl x 101/Rl)F1

Mutation description

• Allele Type: Radiation induced
• Mutation: Deletion
• Oca2^p-4THO-II involves 4 genes/genome features (Oca2, Gabra5, Mir6389 ...) View all
• Mutation details: This deletion is known to encompass the Gabrb3 and the Gabra5 loci. The proximal breakpoint lies within Oca2. (J:29904, J:100221)
• Inheritance: Recessive

Expression

In Mice Carrying this Mutation:

7 assay results

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 4 strains available Cell Lines: 0 lines available
• Carrying any Oca2 Mutation: 70 strains or lines available

References

• Original: J:4101 Nicholls RD, et al., Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):2050-4
• All: 11 reference(s)