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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ptprz1tm1Schl
targeted mutation 1, Joseph Schlessinger
MGI:2386268
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ptprz1tm1Schl/Ptprz1tm1Schl involves: 129 MGI:7484072
hm2
Ptprz1tm1Schl/Ptprz1tm1Schl involves: 129 * Swiss Webster MGI:3029453
cx3
Ptprz1tm1Schl/Ptprz1tm1Schl
Trp53tm1Tyj/Trp53tm1Tyj
involves: 129 * 129S2/SvPas * C57BL/6J MGI:7484075
cx4
Ptprz1tm1Schl/Ptprz1tm1Schl
Trp53tm1Tyj/Trp53+
involves: 129 * 129S2/SvPas * C57BL/6J MGI:7484076
cx5
Ptprz1tm1Schl/Ptprz1+
Trp53tm1Tyj/Trp53+
involves: 129 * 129S2/SvPas * C57BL/6J MGI:7484084


Genotype
MGI:7484072
hm1
Allelic
Composition
Ptprz1tm1Schl/Ptprz1tm1Schl
Genetic
Background
involves: 129
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptprz1tm1Schl mutation (0 available); any Ptprz1 mutation (140 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• mice exhibit spontaneous osteosarcoma development at 18 months of age

skeleton
• mice exhibit spontaneous osteosarcoma development at 18 months of age




Genotype
MGI:3029453
hm2
Allelic
Composition
Ptprz1tm1Schl/Ptprz1tm1Schl
Genetic
Background
involves: 129 * Swiss Webster
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptprz1tm1Schl mutation (0 available); any Ptprz1 mutation (140 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• an increased incidence of apoptosis of mature oligodendrocytes was observed in EAE
• in experimental autoimmune encephalitis (EAE), mutant mice exhibit an impaired ability to recover from demyelinating lesions

immune system




Genotype
MGI:7484075
cx3
Allelic
Composition
Ptprz1tm1Schl/Ptprz1tm1Schl
Trp53tm1Tyj/Trp53tm1Tyj
Genetic
Background
involves: 129 * 129S2/SvPas * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptprz1tm1Schl mutation (0 available); any Ptprz1 mutation (140 available)
Trp53tm1Tyj mutation (12 available); any Trp53 mutation (235 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
N
• contact Xray and histological analysis of undecalcified spine or tibia sections revealed no signs of osteosarcoma development at 12 weeks of age




Genotype
MGI:7484076
cx4
Allelic
Composition
Ptprz1tm1Schl/Ptprz1tm1Schl
Trp53tm1Tyj/Trp53+
Genetic
Background
involves: 129 * 129S2/SvPas * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptprz1tm1Schl mutation (0 available); any Ptprz1 mutation (140 available)
Trp53tm1Tyj mutation (12 available); any Trp53 mutation (235 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• ex vivo, osteosarcoma-derived cell lines exhibit increased proliferation in BrdU incorporation assays, a higher abundance of tyrosine-phosphorylated proteins, and no cellular growth in response to long-term administration of Mdk (midkine, a heparin-binding growth factor known to antagonize Ptprz1 in other cell types)
• at 52 weeks of age, 7 of 38 (~19%) mice exhibit osteosarcoma development by contact X-ray analysis
• skeletal tumors are found in three different locations i.e., ribs, spine or long bones, but not in craniofacial bones, and consist of mineralized tissue
• undecalcified histology showed that tumors represent bony tissue with osteocytes embedded into mineralized matrix, confirming their osteosarcoma nature
• cell lines derived from tumors and cultured in the presence of ascorbic acid and beta-glycerophosphate are able to form a mineralized matrix and show differential expression of osteoblast differentiation markers

skeleton
• at 52 weeks of age, 7 of 38 (~19%) mice exhibit osteosarcoma development by contact X-ray analysis
• skeletal tumors are found in three different locations i.e., ribs, spine or long bones, but not in craniofacial bones, and consist of mineralized tissue
• undecalcified histology showed that tumors represent bony tissue with osteocytes embedded into mineralized matrix, confirming their osteosarcoma nature
• cell lines derived from tumors and cultured in the presence of ascorbic acid and beta-glycerophosphate are able to form a mineralized matrix and show differential expression of osteoblast differentiation markers




Genotype
MGI:7484084
cx5
Allelic
Composition
Ptprz1tm1Schl/Ptprz1+
Trp53tm1Tyj/Trp53+
Genetic
Background
involves: 129 * 129S2/SvPas * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptprz1tm1Schl mutation (0 available); any Ptprz1 mutation (140 available)
Trp53tm1Tyj mutation (12 available); any Trp53 mutation (235 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• at 52 weeks of age, 2 of 38 (~5%) mice exhibit visible skeletal tumors by contact X-ray analysis
• skeletal tumors are found in three different locations i.e., ribs, spine or long bones, but not in craniofacial bones, and consist of mineralized tissue
• cell lines derived from tumors and cultured in the presence of ascorbic acid and beta-glycerophosphate are able to form a mineralized matrix and show differential expression of osteoblast differentiation markers, confirming their osteosarcoma nature

skeleton
• at 52 weeks of age, 2 of 38 (~5%) mice exhibit visible skeletal tumors by contact X-ray analysis
• skeletal tumors are found in three different locations i.e., ribs, spine or long bones, but not in craniofacial bones, and consist of mineralized tissue
• cell lines derived from tumors and cultured in the presence of ascorbic acid and beta-glycerophosphate are able to form a mineralized matrix and show differential expression of osteoblast differentiation markers, confirming their osteosarcoma nature





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last database update
08/21/2024
MGI 6.24
The Jackson Laboratory