rd21
Spontaneous Allele Detail

Summary

• Symbol: rd21
• Name: retinal degeneration 21
• MGI ID: MGI:5906381
• Gene: rd21 Location: unknown Genetic Position: Chr19, Syntenic
• Alliance: rd21 page

Mutation origin

• Strain of Origin: B6.Cg-Tg(FXN*)1Sars Fxn^tm1Mkn/J

Mutation description

• Allele Type: Spontaneous (Not Specified)
• Mutation: Undefined
• This spontaneous mutation has been mapped to Chromosome 19 with close linkage to D19Mit61. (J:242762)
• Inheritance: Recessive

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: 1 strain available Cell Lines: 0 lines available
• Carrying any rd21 Mutation: 1 strain or line available

References

• Original: J:242762 Chang B, et al., A new mouse model of a late onset retinal degeneration (rd21). Invest Ophthalmol Vis Sci. 2015;56(7):2881
• All: 2 reference(s)