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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gulosfx
spontaneous fracture
MGI:2157331
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Gulosfx/Gulosfx BALB/cBy-Gulosfx/J MGI:2174899


Genotype
MGI:2174899
hm1
Allelic
Composition
Gulosfx/Gulosfx
Genetic
Background
BALB/cBy-Gulosfx/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gulosfx mutation (1 available); any Gulo mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• growth plate arrest on the long bones was noted
• osteoid was absent in regions adjacent to the growth plates of the long bones
• necrosis below the growth plate and neovascularization
• lumbar vertebral bodies exhibited an absence of osteoid and trabeculae
• bone mineral density is similar to controls in the center of the femoral diaphysis, but declines significantly at the ends of the femoral diaphysis
• thickness of the mutant bone was approximately 65% of controls
• reduced number of chondrocytes in the growth plates
• reduced osteocalcin levels
• numerous spontaneous impact fractures were observed in mutant mice; complete fractures were less common

homeostasis/metabolism

growth/size/body
• mice failed to maintain the rate of weight gain compared to littermates after 26-30 days of age

hematopoietic system

immune system

behavior/neurological
• mice exhibited increased difficulty moving starting at 26-30 days of age

nervous system

renal/urinary system

reproductive system
N
• normal testis

liver/biliary system

cardiovascular system

integument
• scruffy appearance; possibly due decreased self-grooming behavior

cellular

endocrine/exocrine glands





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
09/03/2024
MGI 6.24
The Jackson Laboratory