Phenotypes Associated with This Genotype

Genotype
MGI:2668613

• Allelic Composition: Nr2e3^rd7/Nr2e3^rd7
• Genetic Background: Not Specified

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

Retinal spotting and degeneration in Nr2e3^rd7/Nr2e3^rd7 mice

vision/eye

retina degeneration ( J:62171 )

• evenly spaced white spots apparent by one month of age

abnormal cone electrophysiology ( J:62171 )

• progressive reduction of cone signals as measures by electroretinographs

• amplitude of signals was 50% of normal by 16 months of age

abnormal rod electrophysiology ( J:62171 )

• progressive reduction of rod signals as measures by electroretinographs

• amplitude of signals was 50% of normal by 16 months of age

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
enhanced S-cone syndrome		DOID:0090059	OMIM:268100	J:62171