cellular
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• loss of heterozygous progeny is seen only when the mutant allele is transmitted from the female parent, suggesting a maternal effect
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Analysis Tools|
Allele Symbol Allele Name Allele ID |
Nfia+ wild type MGI:2434131 |
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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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• loss of heterozygous progeny is seen only when the mutant allele is transmitted from the female parent, suggesting a maternal effect
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• 22% of newborns exhibit hydronephrosis
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• newborns exhibit duplication and dilatation of the ureter at the ureteropelvic junction
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• newborns exhibit duplication and dilatation of the ureter at the ureteropelvic junction
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• some newborns exhibit dilation of the ureterovesical junction
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
Nfiatm1Rmg/Nfia+ Tg(Hoxb7-EGFP)33Cos and Nfiatm1Rmg/Nfiatm1Rmg Tg(Hoxb7-EGFP)33Cos mice have ureteral defects
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• 22% exhibit ureteral development abnormalities that include ureter dilation and partial ureteral duplication
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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 01/06/2026 MGI 6.24 |
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