mortality/aging
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• embryonic lethal, time not speciifed
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Analysis Tools|
Allele Symbol Allele Name Allele ID |
Nmnat1tm1d(EUCOMM)Wtsi targeted mutation 1d, Wellcome Trust Sanger Institute MGI:6272869 |
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| Summary |
2 genotypes
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• embryonic lethal, time not speciifed
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• marker analysis shows loss of both rod and cone photoreceptor outer segments in 12 month old mice
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• by 12 months of age, about 40% of photoreceptors are degenerated
• mice subjected to strong white light for 4 hours show marked photoreceptor degeneration 2 weeks after exposure to light damage
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• retinal degeneration in the outer nuclear layer is seen at 5 months of age
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• ERG on dark-adapted mice under scotopic conditions shows a reduction in the amplitudes of rod-generated a-waves starting at 5 months of age which becomes more pronounced with increasing age
• mice subjected to strong white light for 4 hours show a reduction in scotopic a-wave (rod cells) responses in light-damaged retinas
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• mice subjected to strong white light for 4 hours show a reduction in b-wave (bipolar cells) responses in light-damaged retinas
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• marker analysis shows loss of both rod and cone photoreceptor outer segments in 12 month old mice
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• by 12 months of age, about 40% of photoreceptors are degenerated
• mice subjected to strong white light for 4 hours show marked photoreceptor degeneration 2 weeks after exposure to light damage
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• marker analysis indicates that light-induced retinal damage triggers ER stress
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Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
| Leber congenital amaurosis 9 | DOID:0110005 |
OMIM:608553 |
J:267630 | |
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 09/30/2025 MGI 6.24 |
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