About   Help   FAQ
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
• tumor progression and invasion is delayed
• average tumor size is reduced

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory