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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rhojtm1.2Auem
targeted mutation 1.2, Akiyoshi Uemura
MGI:5608669
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rhojtm1.2Auem/Rhojtm1.2Auem B6.Cg-Rhojtm1.2Auem MGI:5608672
cx2
Rhojtm1.2Auem/Rhojtm1.2Auem
Tg(MMTV-PyVT)634Mul/0
involves: C57BL/6 * CBA/JNCrlj * FVB/N MGI:5608671


Genotype
MGI:5608672
hm1
Allelic
Composition
Rhojtm1.2Auem/Rhojtm1.2Auem
Genetic
Background
B6.Cg-Rhojtm1.2Auem
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rhojtm1.2Auem mutation (0 available); any Rhoj mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• decreased vascular densities, increase in vessel disruptions, and reduced vascular spouting in tumors formed by injection of Lewis lung carcinoma cells
• coverage of tumor vessels with alpha-SMA+ mural cells and basement membrane is decreased and vascular permeability is increased
• vascular densities are also reduced in tumors formed by injected B16F10 melanoma cells
• in tumors formed by injection of Lewis lung carcinoma cells
• tumors formed by injection of Lewis lung carcinoma cells show an increase in hemorrhagic foci and increased hypoxia with extensive apoptosis in the center of the tumor
• decreased growth of injected Lewis lung carcinoma cells
• tumor growth is also delayed for injected B16F10 melanoma cells
• impact of cisplatin, VEGF-A blockade, or combretastatin-A4-phosphate on Lewis lung carcinoma cell tumor growth/necrosis is enhanced compared to wild-type controls

homeostasis/metabolism
• impact of cisplatin on Lewis lung carcinoma cell tumor growth/necrosis is enhanced compared to wild-type controls
• impact of combretastatin-A4-phosphate treatment on inhibition of tumor growth and inhibition of tumor vascularization is enhanced

cardiovascular system
N
• no differences from wild-type controls in vascular morphology or integrity are found in untreated mice
• decreased vascular densities, increase in vessel disruptions, and reduced vascular spouting in tumors formed by injection of Lewis lung carcinoma cells
• coverage of tumor vessels with alpha-SMA+ mural cells and basement membrane is decreased and vascular permeability is increased
• vascular densities are also reduced in tumors formed by injected B16F10 melanoma cells
• tumors formed by injection of Lewis lung carcinoma cells show an increase in hemorrhagic foci




Genotype
MGI:5608671
cx2
Allelic
Composition
Rhojtm1.2Auem/Rhojtm1.2Auem
Tg(MMTV-PyVT)634Mul/0
Genetic
Background
involves: C57BL/6 * CBA/JNCrlj * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rhojtm1.2Auem mutation (0 available); any Rhoj mutation (16 available)
Tg(MMTV-PyVT)634Mul mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• decreased tumor vascular densities and vascular sprouting in peri- and intratumoral regions
• vascular morphology in intratumoral regions appear more disrupted, vascular permeability is increased and pericyte support is reduced
• decreased development of spontaneous mammary tumor nodules at 14 weeks of age and median time to palpable tumor development is delayed by approximately 2 weeks
• average number of metastatic tumor colonies in the lung is reduced
• average tumor size is reduced
• tumor progression and invasion is delayed

homeostasis/metabolism
• 23% delayed wound closure, 48% reduced vascular density and 39% decreased granulation area in wound regions in a punch wound healing assay

cardiovascular system
• decreased tumor vascular densities and vascular sprouting in peri- and intratumoral regions
• vascular morphology in intratumoral regions appear more disrupted, vascular permeability is increased and pericyte support is reduced

endocrine/exocrine glands
• decreased development of spontaneous mammary tumor nodules at 14 weeks of age and median time to palpable tumor development is delayed by approximately 2 weeks

integument
• decreased development of spontaneous mammary tumor nodules at 14 weeks of age and median time to palpable tumor development is delayed by approximately 2 weeks





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
08/02/2024
MGI 6.24
The Jackson Laboratory