Cpfl2
Spontaneous Allele Detail

Summary

• Symbol: Cpfl2
• Name: cone photoreceptor function loss 2
• MGI ID: MGI:3624359
• Gene: Cpfl2 Location: unknown Genetic Position: Chr3, Syntenic
• Alliance: Cpfl2 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 Cpfl2 Mutation: 0 strains or lines available

References

• Original: J:167195 Hawes NL, et al., New Mouse Model of Cone Photoreceptor Function Loss (Cpfl2). Invest Ophthalmol Vis Sci. 2003;44(13):4531
• All: 3 reference(s)