rd22
Spontaneous Allele Detail

Summary

• Symbol: rd22
• Name: retinal degeneration 22
• MGI ID: MGI:7638770
• Gene: rd22 Location: unknown Genetic Position: Chr12, Syntenic
• Alliance: rd22 page

Mutation origin

• Strain of Origin: Not Applicable

Mutation description

• Allele Type: Spontaneous (Not Specified)
• Mutation: Undefined
• Mutation details: This spontaneous mutation mapped to an interval between D12Mit158 and D12Mit133 and has not been proven to be caused by a mutation in Ttll5, but retinal cDNA sequence for Ttll5 shows a G to A point substitution in the 5th base of the 3-prime UTR and a duplication of 122 base pairs beginning at the 7th base pair of the 3-prime UTR. (J:347903)
• Inheritance: Recessive

Disease models

Expression

In Structures Affected by this Mutation:

3 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 rd22 Mutation: 1 strain or line available

References

• Original: J:347903 Chang B, B6.Cg-rd22/BOC strain details. MGI Direct Data Submission. 2024
• All: 1 reference(s)