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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cytiptm1Tes
targeted mutation 1, Lino Tessarollo
MGI:3664082
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cytiptm1Tes/Cytiptm1Tes involves: 129S1/Sv * FVB/N MGI:3715244


Genotype
MGI:3715244
hm1
Allelic
Composition
Cytiptm1Tes/Cytiptm1Tes
Genetic
Background
involves: 129S1/Sv * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cytiptm1Tes mutation (0 available); any Cytip mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• deficient splenocytes injected into wild-type recipients which overexpress Th1 cytokines show lower efficiency in migrating to the spleen
• in a model of aseptic peritonitis, seven days after peritonitis induction, mutants have lower numbers of inflammatory cells in the peritoneal cavity compared to wild-type mice
• in an aseptic peritonitis model, neutrophils display a defect in exiting the circulation into the peritoneal cavity; neutrophils are present in greater numbers in circulation of mutant animals compared to wild-type in aseptic peritonitis model
• after induction of peritonitis in Pscdbp-deficient mice, a limited reduction in circulating WBCs is observed compared to a 50% decrease in wild-type controls
• reduced circulating WBCs in animals >6 months of age, with reduction of neutrophilic and monocytic fractions
• reduced numbers of virus specific CTLs are observed infiltrating the tumors in null mice
• lymphocyte numbers in tumor-draining lymph nodes are significantly reduced compared to controls mice, with fewer leukocytes infiltrating the tumors

hematopoietic system
• deficient splenocytes injected into wild-type recipients which overexpress Th1 cytokines show lower efficiency in migrating to the spleen
• in a model of aseptic peritonitis, seven days after peritonitis induction, mutants have lower numbers of inflammatory cells in the peritoneal cavity compared to wild-type mice
• in an aseptic peritonitis model, neutrophils display a defect in exiting the circulation into the peritoneal cavity; neutrophils are present in greater numbers in circulation of mutant animals compared to wild-type in aseptic peritonitis model
• after induction of peritonitis in Pscdbp-deficient mice, a limited reduction in circulating WBCs is observed compared to a 50% decrease in wild-type controls
• reduced circulating WBCs in animals >6 months of age, with reduction of neutrophilic and monocytic fractions
• reduced numbers of virus specific CTLs are observed infiltrating the tumors in null mice

neoplasm
• in null mice injected with Moloney murine sarcoma/Moloney murine leukemia virus, a higher (but nonsignificant) levelo of tumor incidence is observed (87% vs 70% in controls); mutant animals develop significantly larger sarcomas than wild-type mice
• regression of tumors occurs with slower kinetics than in wild-type controls

cellular
• deficient splenocytes injected into wild-type recipients which overexpress Th1 cytokines show lower efficiency in migrating to the spleen
• in a model of aseptic peritonitis, seven days after peritonitis induction, mutants have lower numbers of inflammatory cells in the peritoneal cavity compared to wild-type mice
• in an aseptic peritonitis model, neutrophils display a defect in exiting the circulation into the peritoneal cavity; neutrophils are present in greater numbers in circulation of mutant animals compared to wild-type in aseptic peritonitis model
• after induction of peritonitis in Pscdbp-deficient mice, a limited reduction in circulating WBCs is observed compared to a 50% decrease in wild-type controls





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
04/23/2024
MGI 6.23
The Jackson Laboratory