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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Rho-GUCY2D*R838S)379Amd
transgene insertion 379, Alexander Dizhoor
MGI:5908875
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
tg1
Tg(Rho-GUCY2D*R838S)379Amd/0 involves: C57BL/6 * C57BL/6J * SJL MGI:6154645


Genotype
MGI:6154645
tg1
Allelic
Composition
Tg(Rho-GUCY2D*R838S)379Amd/0
Genetic
Background
involves: C57BL/6 * C57BL/6J * SJL
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
• erosion of the rod outer segments
• decline in rod photoreceptor function coincides with the progressive degeneration of the photoreceptor cell layer
• reduction of the total count of the photoreceptor nuclei in the outer nuclear layer of the retina is seen by 6 weeks of age and rapidly progresses, so that by 3-4 months of age, less than half and by 6 months, only 1/3 of the photoreceptors remain in the retina
• the average maximal scotopic a-wave is reduced to half the normal amplitude, but the flash strength producing a half-maximal response is not changed
• at 3-6 months of age, the maximal scotopic a-wave amplitude is suppressed 4-fold
• rod-driven scotopic b-wave is reduced in amplitude by 1/3, without a change in half-maximum flash strength
• at 3-6 months of age, the b-wave amplitude is suppressed more than 2-fold
• scotopic ERG in dark-adapted mice exhibit a decline in rod responses as early as 1 month of age
• rod vision further declines between 1 and 3 months of age
• however, cone vision is normal, with normal S-cone and M-cone a-wave and cone b-wave amplitudes
• mice exhibit progressive loss of visual function

nervous system
• erosion of the rod outer segments
• decline in rod photoreceptor function coincides with the progressive degeneration of the photoreceptor cell layer

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cone-rod dystrophy 6 DOID:0111011 OMIM:601777
J:237633





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory