Phenotypes Associated with This Genotype

Genotype
MGI:4867912

• Allelic Composition: Cnga3^cpfl5/Cnga3^cpfl5
• Genetic Background: involves: RHJ/LeJ

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

nervous system

abnormal retina cone cell morphology ( J:167197 )

• migration of the cone somata into the outer plexiform layer of the retina is observed as early as postnatal week 3

vision/eye

abnormal retina cone cell morphology ( J:167197 )

• migration of the cone somata into the outer plexiform layer of the retina is observed as early as postnatal week 3

abnormal cone electrophysiology ( J:166679 , J:167197 )

• no cone ERG response (J:167197)

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
achromatopsia 2		DOID:0110007	OMIM:216900	J:187090