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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
P3h1tm1Dgen
targeted mutation 1, Deltagen
MGI:4830452
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
P3h1tm1Dgen/P3h1tm1Dgen involves: C57BL/6 MGI:4830454


Genotype
MGI:4830454
hm1
Allelic
Composition
P3h1tm1Dgen/P3h1tm1Dgen
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
P3h1tm1Dgen mutation (0 available); any P3h1 mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Reduced body size and skeletal abnormalities in P3h1tm1Dgen/P3h1tm1Dgen mice

skeleton
• the femur exhibit reduced length, bone mineral density, cortical thickness, stiffness, and force to failure compared to in wild-type mice
• the number of small diameter fibrils is increased compared to in wild-type mice
• the distribution of fibril size is altered with more smaller diameter fibrils compared to in wild-type mice
• the chondrocytes within the hypertrophic zone are less organized compared to in wild-type mice
• progressively worsens with age
• in the skull and limbs
• the trabecular area is less mineralized with more spaces compared to in wild-type mice
• at E18 in the parietal bone

growth/size/body
• mice exhibit rhizomelia (decreased ration of femoral length to tibial length) unlike wild-type mice

adipose tissue

muscle
• the number of small diameter fibrils is increased compared to in wild-type mice
• the distribution of fibril size is altered with more smaller diameter fibrils compared to in wild-type mice

limbs/digits/tail
• the femur exhibit reduced length, bone mineral density, cortical thickness, stiffness, and force to failure compared to in wild-type mice

integument
• the dermis is less densely packed compared to in wild-type mice
• normal fibrils are interspersed with clumps of collagen fibrils and gaps and spaces between collagen fibrils unlike in wild-type mice
• thinner and less dense

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
osteogenesis imperfecta type 8 DOID:0110336 OMIM:610915
J:163884





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory