vision/eye
• progressive retina degeneration
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• from 12 months
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Allele Symbol Allele Name Allele ID |
Idh3ampc201H muta-ped-c3pde 201, Harwell MGI:5792025 |
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Summary |
3 genotypes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• progressive retina degeneration
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• from 12 months
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• progressive loss of nuclei in outer nuclear layer (ONL) from age P90
• significantly reduced a-wave amplitude and scotopic ERG response
• no loss of cells at age P60
• normal a-wave amplitude and electroretinogram (ERG) trace at age P60
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• progressive decline in visual acuity by age 12 months, as determined by optokinetic drum (OKD) score
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• loss of significant portion of nuclei in outer nuclear layer (ONL) at age P60, progressing further by P90
• significantly reduced a-wave response and flatline ERG trace at age P60
• normal retinal function at age P30 as determined by electroretinograms (ERGs)
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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 12/10/2024 MGI 6.24 |
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