cpfl7
Spontaneous Allele Detail

Summary

• Symbol: cpfl7
• Name: cone photoreceptor function loss 7
• MGI ID: MGI:3696948
• Gene: cpfl7 Location: unknown Genetic Position: Chr19, Syntenic
• Alliance: cpfl7 page

Mutation origin

• Strain of Origin: Not Specified

Mutation description

• Allele Type: Spontaneous

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 cpfl7 Mutation: 0 strains or lines available

References

• Original: J:167199 Hawes NL, et al., A New Mouse Model of Cone Photoreceptor Fuction Loss (cpfl7). Invest Ophthalmol Vis Sci. 2007;48(13):1350
• All: 2 reference(s)