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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Umodtm1Xrw
targeted mutation 1, Xue-Ru Wu
MGI:3526897
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Umodtm1Xrw/Umodtm1Xrw 129S/SvEv-Umodtm1Xrw MGI:4361712
hm2
Umodtm1Xrw/Umodtm1Xrw B6.129S6-Umodtm1Xrw MGI:5429727
hm3
Umodtm1Xrw/Umodtm1Xrw involves: 129S6/SvEvTac MGI:3527894
ht4
Umodtm1Xrw/Umod+ B6.129S6-Umodtm1Xrw MGI:5429728
cx5
Spp1tm1Blh/Spp1tm1Blh
Umodtm1Xrw/Umodtm1Xrw
129S/SvEv-Spp1tm1Blh Umodtm1Xrw MGI:4361714


Genotype
MGI:4361712
hm1
Allelic
Composition
Umodtm1Xrw/Umodtm1Xrw
Genetic
Background
129S/SvEv-Umodtm1Xrw
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Umodtm1Xrw mutation (0 available); any Umod mutation (5 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• at 2-3 months of age, urine chloride, phosphorus, and calcium phosphate content are higher than in wild-type mice; however, mice exhibit normal urine creatinine, calcium, magnesium, and citrate levels (J:127526)
• at 5-8 months of age, the concentrations of Cl, K, Ca, Mg, P, uric acid, creatinine, and ammonium are nearly doubled relative to wild-type controls (J:163552)
• at 5-8 months of age, mice exhibit urinary supersaturation of calcium phosphate (brushite), uric acid and sodium urate, but not calcium oxalate (J:163552)
• urine chloride ion levels are higher than in wild-type mice (J:127526)
• at 5-8 months of age, the concentrations of organic anions such as citrate and oxalate are slightly lower than in wild-type controls
• at 5-8 months of age, the concentrations of citrate are slightly lower than in wild-type controls
• at 5-8 months of age, urine pH is significantly lower than that in wild-type controls
• urine phosphorus and calcium phosphate levels are higher than in wild-type mice (J:127526)
• under hyperoxaluria conditions, 71% of mice exhibit moderate amounts of calcium crystalluria and renal calcium crystal formation unlike similarly treated wild-type mice
• after 1 month of hyperoxaluria, 15% of mice develop large crystalline deposits at the tip of the renal papillae that can block the proximal portions of the collecting ducts unlike similarly treated wild-type mice
• following hyperoxaluria, mice develop stones unlike similarly treated wild-type mice
• occasionally, large plugging crystals are detected within the ducts of Bellini
• in some mice after 1 month of hyperoxaluria (J:127526)
• when occasional large crystals are found within the ducts of Bellini, adjacent collecting tubules are markedly dilated (J:163552)
• male mice develop progressive renal papillary calcification, unlike wild-type controls
• at 5-8 months of age, 3 of 20 male mice exhibit hydronephrosis
• by 15 months of age, 5 of 16 male mice exhibit hydronephrosis with increased severity
• both unilateral and bilateral hydronephrosis are observed
• 14% of mice exhibit calcifications in the renal papilla unlike wild-type mice (J:127526)
• renal epithelial cells exhibit a 2-fold increase in crystal adhesion to epithelial cells compared with wild-type cells (J:127526)
• 71% of mice exposed to hyperoxaluria develop renal calcinosis unlike similarly treated wild-type mice (J:127526)
• by 5-8 months of age, ~50% of male mice analyzed develop spontaneous renal papillary calcinosis, not observed in wild-type controls; the frequency of crystal deposition in the renal papilla increases to 87.5% by 15 months of age (J:163552)
• at 5-8 months , both intratubular (26.1%) and interstitial calcium crystals (73.9%) are present, while interstitial crystals are even more common (93.2%) by 15 months of age (J:163552)
• papillary interstitial crystals are located primarily beneath the tubular cells of the collecting ducts, and consist of calcium phosphate (hydroxyapatite) and a small amount of calcium carbonate (J:163552)
• the extent of crystal formation varies from tubule to tubule, from small crystals spanning the length of 2-3 tubular cells to large crystals spanning up to 10-15 cells (J:163552)
• no macrophage infiltration is observed in the vicinity of interstitial crystals (J:163552)
• no crystals are detected in the cortex and outer medulla (J:163552)
• following hyperoxaluria, mice exhibit greater renal damage and fibrosis than similarly treated wild-type mice
• most hydronephrotic mice exhibit stone-like structures in the ureter and renal pelvis
• at 5-8 months of age, mice exhibit a significantly lower 24-hr urinary volume than wild-type controls

homeostasis/metabolism
• at 2-3 months of age, urine chloride, phosphorus, and calcium phosphate content are higher than in wild-type mice; however, mice exhibit normal urine creatinine, calcium, magnesium, and citrate levels (J:127526)
• at 5-8 months of age, the concentrations of Cl, K, Ca, Mg, P, uric acid, creatinine, and ammonium are nearly doubled relative to wild-type controls (J:163552)
• at 5-8 months of age, mice exhibit urinary supersaturation of calcium phosphate (brushite), uric acid and sodium urate, but not calcium oxalate (J:163552)
• urine chloride ion levels are higher than in wild-type mice (J:127526)
• at 5-8 months of age, the concentrations of organic anions such as citrate and oxalate are slightly lower than in wild-type controls
• at 5-8 months of age, the concentrations of citrate are slightly lower than in wild-type controls
• at 5-8 months of age, urine pH is significantly lower than that in wild-type controls
• urine phosphorus and calcium phosphate levels are higher than in wild-type mice (J:127526)
• under hyperoxaluria conditions, 71% of mice exhibit moderate amounts of calcium crystalluria and renal calcium crystal formation unlike similarly treated wild-type mice
• after 1 month of hyperoxaluria, 15% of mice develop large crystalline deposits at the tip of the renal papillae that can block the proximal portions of the collecting ducts unlike similarly treated wild-type mice
• following hyperoxaluria, mice develop stones unlike similarly treated wild-type mice




Genotype
MGI:5429727
hm2
Allelic
Composition
Umodtm1Xrw/Umodtm1Xrw
Genetic
Background
B6.129S6-Umodtm1Xrw
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Umodtm1Xrw mutation (0 available); any Umod mutation (5 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• occasionally, large plugging crystals are detected within the ducts of Bellini
• when occasional large crystals are found within the ducts of Bellini, adjacent collecting tubules are markedly dilated
• mice of both sexes develop progressive renal papillary calcification, unlike wild-type controls
• at 5-8 months of age, 2 of 9 male mice and 1 of 11 female mice exhibit hydronephrosis
• by 15 months of age, 7 of 11 male mice and 2 of 2 female mice exhibit hydronephrosis with increased severity
• both unilateral and bilateral hydronephrosis are observed
• by 5-8 months of age, ~50% of mice (both sexes analyzed) develop spontaneous renal papillary calcinosis, not observed in wild-type controls; the frequency of crystal deposition in the renal papilla increases to 100% in both sexes by 15 months of age
• at 5-8 months, both intratubular (26.1%) and interstitial calcium crystals (73.9%) are present, while interstitial crystals are even more common (93.2%) by 15 months of age
• papillary interstitial crystals are located primarily beneath the tubular cells of the collecting ducts, and consist of calcium phosphate (hydroxyapatite) and a small amount of calcium carbonate
• the extent of crystal formation varies from tubule to tubule, from small crystals spanning the length of 2-3 tubular cells to large crystals spanning up to 10-15 cells
• no macrophage infiltration is observed in the vicinity of interstitial crystals
• no crystals are detected in the cortex and outer medulla
• most hydronephrotic mice exhibit stone-like structures in the ureter and renal pelvis




Genotype
MGI:3527894
hm3
Allelic
Composition
Umodtm1Xrw/Umodtm1Xrw
Genetic
Background
involves: 129S6/SvEvTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Umodtm1Xrw mutation (0 available); any Umod mutation (5 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• intravesicular inoculation of type 1-fimbriated E.coli, but not type P-fimbriated E.coli, caused significantly greater bladder colonization than in controls, indicating susceptibility to bladder infection by type 1-fimbriated E.coli




Genotype
MGI:5429728
ht4
Allelic
Composition
Umodtm1Xrw/Umod+
Genetic
Background
B6.129S6-Umodtm1Xrw
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Umodtm1Xrw mutation (0 available); any Umod mutation (5 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• at 5-8 months of age, 2 of 18 male mice but none of 8 female mice exhibit hydronephrosis
• by 15 months of age, 3 of 4 male mice and 1 of 3 female mice exhibit hydronephrosis with increased severity
• both unilateral and bilateral hydronephrosis are observed
• at 5-8 months of age, 33.3% of male and 25% of female mice exhibit spontaneous renal papillary calcinosis
• by 15 months of age, 75% of male and 33.3% of female mice develop renal papillary calcium crystallization
• most hydronephrotic mice exhibit stone-like structures in the ureter and renal pelvis




Genotype
MGI:4361714
cx5
Allelic
Composition
Spp1tm1Blh/Spp1tm1Blh
Umodtm1Xrw/Umodtm1Xrw
Genetic
Background
129S/SvEv-Spp1tm1Blh Umodtm1Xrw
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Spp1tm1Blh mutation (2 available); any Spp1 mutation (40 available)
Umodtm1Xrw mutation (0 available); any Umod mutation (5 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• urine phosphorus and calcium phosphate content are higher than in wild-type mice
• under hyperoxaluria conditions, 95% of mice exhibit large amounts of calcium crystalluria and renal calcium crystal formation unlike similarly treated wild-type mice
• after 1 month of hyperoxaluria, 18% of mice develop large crystalline deposits at the tip of the renal papillae that can block the proximal portions of the collecting ducts unlike similarly treated wild-type mice
• following hyperoxaluria, mice develop stones unlike similarly treated wild-type mice
• in some mice after 1 month of hyperoxaluria
• 95% of mice exposed to hyperoxaluria develop renal calcinosis unlike similarly treated wild-type mice
• 39% of mice exhibit calcifications in the renal papilla unlike wild-type mice
• renal epithelial cells exhibit a 3.5-fold increase in crystal adhesion to epithelial cells compared with wild-type cells
• following hyperoxaluria, mice exhibit greater renal damage and fibrosis than similarly treated wild-type mice

homeostasis/metabolism
• urine phosphorus and calcium phosphate content are higher than in wild-type mice
• under hyperoxaluria conditions, 95% of mice exhibit large amounts of calcium crystalluria and renal calcium crystal formation unlike similarly treated wild-type mice
• after 1 month of hyperoxaluria, 18% of mice develop large crystalline deposits at the tip of the renal papillae that can block the proximal portions of the collecting ducts unlike similarly treated wild-type mice
• following hyperoxaluria, mice develop stones unlike similarly treated wild-type mice





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last database update
07/05/2024
MGI 6.24
The Jackson Laboratory