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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Magi2tm1.1Knis
targeted mutation 1.1, Katsuhiko Nishimori
MGI:5439615
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Magi2tm1.1Knis/Magi2tm1.1Knis Not Specified MGI:5660913


Genotype
MGI:5660913
hm1
Allelic
Composition
Magi2tm1.1Knis/Magi2tm1.1Knis
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Magi2tm1.1Knis mutation (0 available); any Magi2 mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygous mutant pups die within 48 hours after birth; no homozygotes survive to weaning age
• however, gross appearance as well as body and organ weights remain normal

homeostasis/metabolism
• neonates exhibit a 4-fold increase in plasma creatinine levels relative to wild-type controls

renal/urinary system
• neonates exhibit abnormal morphology of podocyte foot processes; the distance between foot processes is dramatically reduced
• foot processes are shortened, and the interdigitating network appears disorganized
• fusion of the podocyte foot processes results in loss of normal slit diaphragm structure
• no clear slit diaphragms are observed, due to fusion and/or adhesion of the foot processes
• neonates display a lack of urine in the bladder, indicating severe impairment of renal function





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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
09/24/2024
MGI 6.24
The Jackson Laboratory