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Phenotypes Associated with This Genotype
Genotype
MGI:2668613
Allelic
Composition
Nr2e3rd7/Nr2e3rd7
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nr2e3rd7 mutation (2 available); any Nr2e3 mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Retinal spotting and degeneration in Nr2e3rd7/Nr2e3rd7 mice

vision/eye
• evenly spaced white spots apparent by one month of age (J:62171)
• evenly spaced white spots apparent by one month of age (J:62171)
• progressive reduction of cone signals as measures by electroretinographs (J:62171)
• amplitude of signals was 50% of normal by 16 months of age (J:62171)
• progressive reduction of cone signals as measures by electroretinographs (J:62171)
• amplitude of signals was 50% of normal by 16 months of age (J:62171)
• progressive reduction of rod signals as measures by electroretinographs (J:62171)
• amplitude of signals was 50% of normal by 16 months of age (J:62171)
• progressive reduction of rod signals as measures by electroretinographs (J:62171)
• amplitude of signals was 50% of normal by 16 months of age (J:62171)

Mouse Models of Human Disease
OMIM ID Ref(s)
Enhanced S-Cone Syndrome; ESCS 268100 J:62171


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/02/2016
MGI 6.02
The Jackson Laboratory