About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rap1atm1Tze
targeted mutation 1, Tomasz Zemojtel
MGI:3830343
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rap1atm1Tze/Rap1atm1Tze involves: 129P2/OlaHsd * C57BL/6 MGI:3830358


Genotype
MGI:3830358
hm1
Allelic
Composition
Rap1atm1Tze/Rap1atm1Tze
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rap1atm1Tze mutation (0 available); any Rap1a mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• splenocytes and thymocytes have lower adhesion to fibronectin coated plates
• only half as many splenocytes adhere after 30 minutes compared to controls
• adherence to ICAM was also less than controls, with larger differences observed upon activation
• both T and B cells demonstrate decreased ability to bind to ICAM compared to controls
• T cells stimulated by anti-CD3 treatment have much less proliferation than wild-type controls
• there is also less proliferation than controls in response to anti-CD3/CD28 stimulation
• activated T cells secrete less IL-2 than wild-type controls with the biggest difference occurring with anti-CD3 stimulation

hematopoietic system
• splenocytes and thymocytes have lower adhesion to fibronectin coated plates
• only half as many splenocytes adhere after 30 minutes compared to controls
• adherence to ICAM was also less than controls, with larger differences observed upon activation
• both T and B cells demonstrate decreased ability to bind to ICAM compared to controls
• T cells stimulated by anti-CD3 treatment have much less proliferation than wild-type controls
• there is also less proliferation than controls in response to anti-CD3/CD28 stimulation

cellular
• splenocytes and thymocytes have lower adhesion to fibronectin coated plates
• only half as many splenocytes adhere after 30 minutes compared to controls
• adherence to ICAM was also less than controls, with larger differences observed upon activation
• both T and B cells demonstrate decreased ability to bind to ICAM compared to controls
• T cells stimulated by anti-CD3 treatment have much less proliferation than wild-type controls
• there is also less proliferation than controls in response to anti-CD3/CD28 stimulation





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
11/19/2024
MGI 6.24
The Jackson Laboratory