nervous system
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• prosencephalon is truncated
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Analysis Tools|
Allele Symbol Allele Name Allele ID |
Six3tm2.1Gco targeted mutation 2.1, Guillermo Oliver MGI:3693322 |
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| Summary |
3 genotypes
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• prosencephalon is truncated
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• defects are observed starting at E10.5
• reduction in size of invaginating lens pit is observed in mildly and moderately affected embryos
• at E14.5, some embryos have an abnormally persistent lens stalk
• differentiation of lens is not affected in mildly or moderately affected mutant lenses
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• in severely affected lenses at E10.5, no lens-like structures are present
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• at E12.5, in mild cases, lens vesicle is small but relatively normal, small and abnormal in moderated cases and completely absent in severely affected embryos and neuroretinal is malformed also
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• at E14.5 some embryos show disorganized lens fibers
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• some mice show drastically reduced lens size
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• shape of vesicle is defective
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• some embryos injected with tamoxifen early show defective forebrain patterning
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• when tamoxifen is given at E7.5 and 8.5, no thickening or invagination of the PLE is observed at least in one side
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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 09/30/2025 MGI 6.24 |
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