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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cnga3cpfl5
cone photoreceptor function loss 5
MGI:3608770
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cnga3cpfl5/Cnga3cpfl5 B6.RHJ-Cnga3cpfl5/BocJ MGI:5796753
hm2
Cnga3cpfl5/Cnga3cpfl5 involves: RHJ/LeJ MGI:4867912


Genotype
MGI:5796753
hm1
Allelic
Composition
Cnga3cpfl5/Cnga3cpfl5
Genetic
Background
B6.RHJ-Cnga3cpfl5/BocJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cnga3cpfl5 mutation (1 available); any Cnga3 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• moderate cone loss in the outer segment by 5 months of age
• by 3 weeks of age S-opsin immunostaining of the retina is decreased, by 5 weeks of age PNA staining of retinal sections shows decreased cone densities outside the superior hemisphere, primarily in the nasal inferior quadrant, consistent with loss of S-cones, and by 10 weeks of age no S-opsin staining is found
• at 3 weeks of age staining intensity and localization of M-opsin is normal in immunohistochemistry of retinal sections, but by 10 weeks of age M-opsin is found mislocalized to cone inner segments, nuclei, and synaptic termini
• at 5.5 months of age rod-mediated ERG responses at 0.43 log cd-s per m2 are lower than that of C57BL/6J controls
• light-adapted single stimulus ERG at either 1.08 or 0.65 log cd-s/m2 at 5 weeks of age gave no b-wave, consistent with retinal cone cell degeneration
• optomoter behavioral analysis shows decreased visual acuities of 0.273 cycles per degree at 5.5 months of age
• contrast sensitivities tested at a spatial frequency of 0.256 cycles/degree at 5.5 months of age are decreased relative to C57BL/6J controls

nervous system
• moderate cone loss in the outer segment by 5 months of age
• by 3 weeks of age S-opsin immunostaining of the retina is decreased, by 5 weeks of age PNA staining of retinal sections shows decreased cone densities outside the superior hemisphere, primarily in the nasal inferior quadrant, consistent with loss of S-cones, and by 10 weeks of age no S-opsin staining is found
• at 3 weeks of age staining intensity and localization of M-opsin is normal in immunohistochemistry of retinal sections, but by 10 weeks of age M-opsin is found mislocalized to cone inner segments, nuclei, and synaptic termini

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




Genotype
MGI:4867912
hm2
Allelic
Composition
Cnga3cpfl5/Cnga3cpfl5
Genetic
Background
involves: RHJ/LeJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cnga3cpfl5 mutation (1 available); any Cnga3 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• migration of the cone somata into the outer plexiform layer of the retina is observed as early as postnatal week 3

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





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory