Phenotypes associated with this allele

• Allele Symbol: cpfl7
• Allele Name: cone photoreceptor function loss 7
• Allele ID: MGI:3696948
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	cpfl7/cpfl7	Not Specified	MGI:4867851

Genotype
MGI:4867851

hm1

• Allelic Composition: cpfl7/cpfl7
• Genetic Background: Not Specified

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

vision/eye

abnormal retina ganglion cell morphology ( J:167199 )

• ganglion cell disruption

retina degeneration ( J:167199 )

• retinal segment degeneration in the peripheral retina at 3 months of age

abnormal cone electrophysiology ( J:166679 , J:167199 )

• lower b-wave dark adapted ERG response starting at 3 weeks of age (J:167199)

• normal a-wave light adapted ERG response (J:167199)

behavior/neurological

limb grasping ( J:167199 )

• leg clasping when lifted by the tail

abnormal gait ( J:167199 )

• high stepping gait when walking on shavings

nervous system

abnormal retina ganglion cell morphology ( J:167199 )

• ganglion cell disruption