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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Sosttm1Paz
targeted mutation 1, Chris Paszty
MGI:3850014
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Sosttm1Paz/Sosttm1Paz involves: 129/Sv * Black Swiss MGI:3850032
cx2
Lrp5tm1Grw/Lrp5tm1Grw
Sosttm1Paz/Sosttm1Paz
involves: 129S1/Sv * 129X1/SvJ * Black Swiss MGI:5632201


Genotype
MGI:3850032
hm1
Allelic
Composition
Sosttm1Paz/Sosttm1Paz
Genetic
Background
involves: 129/Sv * Black Swiss
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sosttm1Paz mutation (0 available); any Sost mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• osteoblast surface is increased 1007% in males and 189% in females compared to in wild-type mice

skeleton
• osteoblast surface is increased 1007% in males and 189% in females compared to in wild-type mice
• female mice exhibit a slightly longer femur than wild-type females
• mice exhibit increased radiodensity throughout the skeleton compared to in wild-type mice (J:150166)
• whole body bone mineral density is increased (J:213541)
• areal bone mineral density in male mice is increased 62% for lumbar vertebrae and 55% for the whole leg compared with wild-type mice
• muCT analysis of distal femoral metaphysis and femur shaft shows increase in trabecular volumetric bone mineral density (+149% in males and +281% in female) compared to wild-type
• bone volume fraction (BV/TV) is increased
• static histomorphometric analysis shows increased cortical area (+78% in males and +55% in females) and periosteal perimeter (+17% in males, +21% in females) compared to in wild-type mice
• static histomorphometric analysis shows decreased endocortical perimeter (-20% in males and -14% in females) compared to in wild-type mice
• the metaphyseal region of distal femur exhibits an increase in trabecular bone compared to in wild-type mice
• static histomorphometric analysis shows that trabecular bone volume is increased (+237% in males and +391% in females) compared to in wild-type mice
• muCT analysis of distal femoral metaphysis and femur shaft shows increase in trabecular bone volume (+146% in males and +224% in females) compared to in wild-type mice
• static histomorphometric analysis shows that trabecular number is increased (+37% in males and +57% in females) compared to in wild-type mice
• static histomorphometric analysis shows that trabecular thickness is increased (+146% in males and +219% in females) compared to in wild-type mice
• dynamic histomorphometric analysis of the femur midshaft shows increased cortical bone formation with increase periosteal mineralization surface (+194% in males, 249% in females), periosteal mineral apposition rate (143% in males), periosteal bone formation rate (+396% in males), endocortical minearal apposition rate (+1402% in males, +269% in females), endocortical mineral apposition rate (+1249% in males, +102% in females), and endocortical bone formation (+7891% in males and +499% in females) compared to in wild-type mice
• bone volume is increased in the trabecular and cortical compartments compared to in wild-type mice
• mineral apposition rates and bone formation rates are increased
• in a compression testing, lumbar vertebrae exhibit a higher maximum load (+243% in males and +188% in females), stiffness (+93% in males), and energy failure (+415% in males and +556% in females) compared to in wild-type mice (J:150166)
• in a three-point bend testing, femur diaphysis exhibit a higher maximum load (+132% in males and +154% in females), stiffness (+87% in males and +119% in females), and energy failure (+83% in males and +198% in females) compared to in wild-type mice (J:150166)
• bones show increased ultimate force, energy to failure, and stiffness, indicating enhanced bone strength (J:213541)

growth/size/body
• female mice exhibit a slightly higher body weight than wild-type females

limbs/digits/tail
• female mice exhibit a slightly longer femur than wild-type females

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
sclerosteosis 1 DOID:0060756 OMIM:269500
J:213541




Genotype
MGI:5632201
cx2
Allelic
Composition
Lrp5tm1Grw/Lrp5tm1Grw
Sosttm1Paz/Sosttm1Paz
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * Black Swiss
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lrp5tm1Grw mutation (1 available); any Lrp5 mutation (82 available)
Sosttm1Paz mutation (0 available); any Sost mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• mice exhibit bone mineral content that is greater than in single Lrp5 homozygotes and intermediate between those of wild-type and single Sost homozygotes
• mice exhibit whole-body mineral density that is greater than in single Lrp5 homozygotes and intermediate between those of wild-type and single Sost homozygotes
• however, mineral apposition rates and bone formation rates do not differ from wild-type mice but are increased compared to single Lrp5 homozygotes
• mice exhibit bone volume fraction (BV/TV) values that are greater than in single Lrp5 homozygotes and are intermediate between those of wild-type and single Sost homozygotes
• females exhibit a greater increase in BV/TV than male mice
• females exhibit a greater increase in trabecular number than male mice
• increase in bone stiffness compared to wild-type mice and single Lrp5 homozygotes
• bones show increased ultimate force, energy to failure, and stiffness, indicating enhanced bone strength compared to wild-type mice and single Lrp5 homozygotes





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory