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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tcf21tm2.1Seq
targeted mutation 2.1, Susan E Quaggin
MGI:5613240
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Tcf21tm2.1Seq/Tcf21tm1Jrt
Tg(Nphs2-cre)1Seq/0
involves: 129S1/Sv * 129X1/SvJ MGI:5613385
cn2
Tcf21tm2.1Seq/Tcf21tm1Jrt
Wnt4tm2(EGFP/cre)Svo/Wnt4+
involves: 129S1/Sv * 129X1/SvJ MGI:5613386


Genotype
MGI:5613385
cn1
Allelic
Composition
Tcf21tm2.1Seq/Tcf21tm1Jrt
Tg(Nphs2-cre)1Seq/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tcf21tm1Jrt mutation (0 available); any Tcf21 mutation (14 available)
Tcf21tm2.1Seq mutation (0 available); any Tcf21 mutation (14 available)
Tg(Nphs2-cre)1Seq mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• significantly increased urinary protein to creatinine ratio in affected mice
• streptozotocin induced diabetes at 17 weeks of age in protected cohort results in increased urinary protein to creatinine ratio
• massive proteinuria in 40% of mice by 5 weeks of age
• 60& of mice do not develop proteinuria through 8 months of age
• in protected cohort of mice proteinuria development resumes after 32 weeks of age
• streptozotocin induced diabetes at 17 weeks of age in protected cohort results in massive proteinuria
• dynamic proliferation of cells in Bowman's capsule
• occasional podocyte vacuolation
• focal flattening and disorganized foot processes in all mice
• extensive effacement in affected mice with large bumpy subepithelial protrusions of the glomerular basement membrane
• prominent fibrinogen depositions
• simplified glomerular structure at birth and at 3 weeks of age
• total cell number reduced by 15%
• non-podocyte cell number reduced 25%
• focal and segmental glomerulosclerosis with occasional crescent formation and podocyte vacuolation
• streptozotocin induced diabetes at 17 weeks of age in protected cohort results in dramatic glomerulosclerosis
• with an irregular surface in affected mice
• in affected mice
• end stage renal disease in some mice with death at 3-6 weeks of age

homeostasis/metabolism
• significantly increased urinary protein to creatinine ratio in affected mice
• streptozotocin induced diabetes at 17 weeks of age in protected cohort results in increased urinary protein to creatinine ratio
• massive proteinuria in 40% of mice by 5 weeks of age
• 60& of mice do not develop proteinuria through 8 months of age
• in protected cohort of mice proteinuria development resumes after 32 weeks of age
• streptozotocin induced diabetes at 17 weeks of age in protected cohort results in massive proteinuria




Genotype
MGI:5613386
cn2
Allelic
Composition
Tcf21tm2.1Seq/Tcf21tm1Jrt
Wnt4tm2(EGFP/cre)Svo/Wnt4+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tcf21tm1Jrt mutation (0 available); any Tcf21 mutation (14 available)
Tcf21tm2.1Seq mutation (0 available); any Tcf21 mutation (14 available)
Wnt4tm2(EGFP/cre)Svo mutation (1 available); any Wnt4 mutation (20 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• defective foot process formation
• podocytes remain columnar at E18.5
• glomeruli are primitive and reduced in size at E18.5
• complexity of glomerulus is reduced
• slightly reduced in size but no overt abnormality in tubular formation





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory