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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(RBP3-ELOVL4*)3Kzh
transgene insertion 3, Kang Zhang
MGI:4360793
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
tg1
Tg(RBP3-ELOVL4*)3Kzh/0 C57BL/6-Tg(RBP3-ELOVL4*)3Kzh MGI:4360798


Genotype
MGI:4360798
tg1
Allelic
Composition
Tg(RBP3-ELOVL4*)3Kzh/0
Genetic
Background
C57BL/6-Tg(RBP3-ELOVL4*)3Kzh
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• abnormalities are more evident as expression levels of the transgene increase in the three lines created
• mice exhibit localized regions of the retina that appear lighter because of depigmentation in areas of retinal pigment epithelium atrophy and photoreceptor degeneration
• as early as 3 weeks, the photoreceptor outer segment is severely stunted with disks clustered in groups instead of stacked as in wild-type mice
• at 6 weeks, 50% of photoreceptor in the outer nuclear layer are degenerated
• more severe in the center of the retina
• retinal degeneration is progressive, localized, and more severe in the center of the retina
• retinal degeneration is more severe than in other lines over expressing the same transgene
• at rod-saturation, cone b-wave declines in amplitude compared to in wild-type mice
• rod b-wave response is reduced at 22 weeks and absent at 22 weeks

nervous system
• as early as 3 weeks, the photoreceptor outer segment is severely stunted with disks clustered in groups instead of stacked as in wild-type mice
• at 6 weeks, 50% of photoreceptor in the outer nuclear layer are degenerated

pigmentation
• more severe in the center of the retina

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Stargardt disease DOID:0050817 OMIM:248200
OMIM:600110
OMIM:603786
J:97173





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory