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Phenotypes Associated with This Genotype
Genotype
MGI:3611443
Allelic
Composition
Wt1tm2Hst/Wt1+
Genetic
Background
chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Wt1tm2Hst mutation (0 available); any Wt1 mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• the XXY heterozygous male had aspermic epididymides
(J:53585)
(J:103489)
• male sex reversal does not occur, however, only 2 of 23 XX to XY chimeras developed as phenotypic males, a significantly lower proportion than the 40% found in wild-type XX to XY chimeras, indicating that the sex ratio is distorted
• a single heterozygous male, that is 41, XXY, was obtained from a female chimera and is sterile

renal/urinary system
• kidneys of the heterozygous male exhibit a secondary hypertensive nephropathy, indicating kidney disease
• exhibit interlobular arteries with severe hypertensive damage, including fibrinoid necrosis, medial hypertrophy and hyperplasia, and loss of the arterial lumen
• obliteration of the glomerular capillary bed
• mesangial cells show an increase in nuclear size, a prominent nucleolus, and hypercellularity
• mesangial hypercellularity
• kidneys of the heterozygous male exhibit tubular epithelial microcyst formation
• obliteration of the urinary filtration space
• podocytes show loss of foot processes
• podocyte hypertrophy and hyperplasia
• podocytes show microvillus transformation of the apical surface
• kidneys of the heterozygous male and of chimeras, although to a lesser extent than the heterozygote, exhibit a diffuse and global mesangial sclerosis, indicating kidney disease
• global sclerosis of the glomerular tuft and obliteration of the glomerular capillary bed and urinary filtration space by an increase in extracellular mesangial matrix
• glomerulus shows focal crescent formation
• the male heterozygote exhibits end-stage renal failure at 8 months of age

endocrine/exocrine glands
(J:53585)
(J:103489)

cardiovascular system
• kidneys of the heterozygous male exhibit a secondary hypertensive nephropathy, indicating kidney disease
• exhibit interlobular arteries with severe hypertensive damage, including fibrinoid necrosis, medial hypertrophy and hyperplasia, and loss of the arterial lumen
• obliteration of the glomerular capillary bed

cellular
• the XXY heterozygous male had aspermic epididymides
• mesangial cells show an increase in nuclear size, a prominent nucleolus, and hypercellularity
• mesangial hypercellularity

growth/size/body
• kidneys of the heterozygous male exhibit tubular epithelial microcyst formation

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Denys-Drash syndrome DOID:3764 OMIM:194080
J:53585 , J:103489


Contributing Projects:
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
11/19/2024
MGI 6.24
The Jackson Laboratory