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Phenotypes Associated with This Genotype
Genotype
MGI:5514055
Allelic
Composition
Ostm1om/Ostm1om
Genetic
Background
C3HeB/FeJ-Ostm1om
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ostm1om mutation (1 available); any Ostm1 mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• however, provision with soft food improves survival
• shortened life span in some mice

skeleton
• at P14, P21 and P30 to P32, some mice exhibit small or thinner teeth or missing incisors
• most incisors erupt but appear damaged and degenerate within the first month of life
• molars are not regularly aligned
• upper molar 3 appears damaged
• some molars are still covered with bone and an epithelial cell layer
• most molars fail to erupt
• rough appearance around the roots of damaged upper incisors
• sclerosis in the maxillary area
• the zygomatic process of the maxilla is thicker and continues to be thick halfway into the zygomatic bone compared to in wild-type mice
• layered appearance
• increased density and abnormal morphology
• increased density of the diaphyses in female mice
• increased density at the distal epiphysis
• thick proximal ribs 1 through 8, especially on the dorsal parts
• full body, femur or right knee in female mice at 8 and 12 weeks
• in male mice at 8 but not 12 weeks
• in the jaw, the compact bone is invaded by blood vessels and has a very irregular structure
• disorganized in the jaw
• progressive in female, but not male, mice

craniofacial
• at P14, P21 and P30 to P32, some mice exhibit small or thinner teeth or missing incisors
• most incisors erupt but appear damaged and degenerate within the first month of life
• molars are not regularly aligned
• upper molar 3 appears damaged
• some molars are still covered with bone and an epithelial cell layer
• most molars fail to erupt
• rough appearance around the roots of damaged upper incisors
• sclerosis in the maxillary area
• the zygomatic process of the maxilla is thicker and continues to be thick halfway into the zygomatic bone compared to in wild-type mice

homeostasis/metabolism
• likely due to poor nutritional status
• likely due to poor nutritional status

growth/size/body
• at P14, P21 and P30 to P32, some mice exhibit small or thinner teeth or missing incisors
• most incisors erupt but appear damaged and degenerate within the first month of life
• molars are not regularly aligned
• upper molar 3 appears damaged
• some molars are still covered with bone and an epithelial cell layer
• most molars fail to erupt
• around time of weaning

adipose tissue

pigmentation
• more grey less yellow coat color

hematopoietic system
• likely due to poor nutritional status

integument
• more grey less yellow coat color

limbs/digits/tail
• increased density and abnormal morphology
• increased density of the diaphyses in female mice
• increased density at the distal epiphysis


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
03/18/2025
MGI 6.24
The Jackson Laboratory