Crygc^MNU8
Chemically induced Allele Detail

Summary

• Symbol: Crygc^MNU8
• Name: crystallin, gamma C; MNU8
• MGI ID: MGI:3578335
• Gene: Crygc Location: Chr1:65110684-65112691 bp, - strand Genetic Position: Chr1, 32.81 cM
• Alliance: Crygc^MNU8 page

Mutation origin

• Strain of Origin: Not Specified

Mutation description

• Allele Type: Chemically induced (other)
• Mutation: Single point mutation
• Mutation details: A G to A transition causes a TRP157 to stop codon change, truncating the transcript by 15 amino acids. (J:90087)
• Inheritance: Not Specified

Expression

In Structures Affected by this Mutation:

2 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 Crygc Mutation: 13 strains or lines available

Notes

The strain of origin is either (102/ElxC3H/El)F1 or DBA/2

References

• Original: J:90087 Graw J, et al., Genetic and allelic heterogeneity of Cryg mutations in eight distinct forms of dominant cataract in the mouse. Invest Ophthalmol Vis Sci. 2004 Apr;45(4):1202-13
• All: 1 reference(s)