Phenotypes associated with this allele

• Allele Symbol: Cpfl2
• Allele Name: cone photoreceptor function loss 2
• Allele ID: MGI:3624359
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
ot1	Cpfl2/?	Not Specified	MGI:4867901

Genotype
MGI:4867901

ot1

• Allelic Composition: Cpfl2/?
• Genetic Background: Not Specified

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

vision/eye

abnormal retina morphology ( J:167195 )

• large waves and rosettes are present in the central retina at 8 months of age

retina spots ( J:167195 )

• retinal spots appear around the optic head at 4 months of age and progress to cover the entire retina by 7 months of age

abnormal cone electrophysiology ( J:166679 , J:167195 )

• cone-mediated photoresponses start to decrease at 2 months of age and are gone by 4 months of age (J:167195)

• rod-mediated photoresponses are normal from 3 weeks to 8 months of age (J:167195)