Allele Symbol Allele Name Allele ID |
Frem2my myelencephalic blebs MGI:1856964 |
Summary |
3 genotypes |
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• renal agenesis
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• some acephalic and extremely pale embryos are found and these are born dead
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• a clear lesion in the region of the eye is generally found at birth and the severity is greatly variable extending to degeneration of the eye elements
(J:14847)
• in cases where only one eye is abnormal it can be the left or right with no preference for one or the other
(J:14847)
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• shortened foreface and considerable variation in the length and shape of the foreface can be found
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• in some stillborn
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• in addition to the eye and facial defects the feet and legs can be impacted to varying degrees including absent, shortened, or malformed digits, hemorrhagic lesions on the digits and legs, twisted foot or paw, or badly distorted leg
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• of the middle digits
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• shortened foreface and considerable variation in the length and shape of the foreface can be found
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• Background Sensitivity: many systems are affected with variable penetrance
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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 03/25/2025 MGI 6.24 |
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