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Phenotypes Associated with This Genotype
Genotype
MGI:5922030
Allelic
Composition
Aipl1tvrm119/Aipl1tvrm119
Genetic
Background
C57BL/6J-Aipl1tvrm119/Pjn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aipl1tvrm119 mutation (1 available); any Aipl1 mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• rapid photoreceptor degeneration is not evident at 8 or 12 days of age, but by 1 month of age only one layer of photoreceptor nuclei remain

vision/eye
• rapid photoreceptor degeneration is not evident at 8 or 12 days of age, but by 1 month of age only one layer of photoreceptor nuclei remain
• dark-adapted ERG response amplitudes are reduced at 18 days of age

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Leber congenital amaurosis 4 DOID:0110332 OMIM:604393
J:243745


Contributing Projects:
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
03/24/2020
MGI 6.15
The Jackson Laboratory