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Phenotypes Associated with This Genotype
Genotype
MGI:5049915
Allelic
Composition
Phospho1m1Jlm/Phospho1m1Jlm
Genetic
Background
involves: C3HeB/FeJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Phospho1m1Jlm mutation (0 available); any Phospho1 mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• skeletal defects are not rescued by over-expression of Alpl
• evident at 1 month of age and becoming worse with age
• evident at 1 month of age and becoming worse with age
• at 1 month of age, mice exhibit dextro- and levoscoliosis that becomes worse with age unlike in wild-type mice
• in the cortical bone of the femur, tibia, and humerus
• Ashing analysis showed decreased bone mineral density in the humerus
• cortical bone mineral density is significantly reduced in the femur
• in the medular cavity of the tibia
• mice exhibit increased cortical porosity in the femur compared with wild-type mice
• mice exhibit decreased trabecular spacing in the medular cavity of the tibia compared to in wild-type mice
• in the medular cavity of the tibia
• in the trabecular bone
• at P10, some mice exhibit a complete absence of secondary ossification centers unlike wild-type mice
• from P1, mice develop greenstick fractures in vertebrae and hind and fore limbs unlike wild-type mice
• chondrocytes exhibit reduced mineralizing ability compared with wild-type cells
• chondrocyte-derived matrix vesicles exhibit reduced calcification ability compared with wild-type vesicles

behavior/neurological

growth/size/body
• more prominent at 2 months in male and female mice

homeostasis/metabolism

limbs/digits/tail
• Ashing analysis showed decreased bone mineral density in the humerus


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
04/30/2024
MGI 6.23
The Jackson Laboratory