About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:4834471
Allelic
Composition
Ptprctm1Mak/Ptprctm1Mak
Genetic
Background
B6.Cg-Ptprctm1Mak
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptprctm1Mak mutation (2 available); any Ptprc mutation (212 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• intestinal intraepithelial lymphocytes (iIELs) exhibit increased spontaneous apoptosis compared to in wild-type mice
• gamma-delta iIELs are more susceptible to induction of apoptosis compared with alpha-beta iIELs
• intestinal intraepithelial lymphocytes (iIELs) is impaired
• however, extrathymic development of iIELs is normal in reconstitution experiments
• intestinal intraepithelial lymphocytes (iIELs) are slightly larger than wild-type cells
• in reconstitution experiments, intrathymic development of iIELs is impaired
• however, extrathymic development of iIELs is normal in reconstitution experiments
• at 10 weeks, the number of intestinal intraepithelial lymphocytes (iIELs) is increased 1.5- to 2-fold compared to in wild-type mice
• at 10 weeks, the number of CD4+CD8- alpha-beta iIELs is increased 7-fold compared to in wild-type mice
• the number of iIELs decrease over time unlike in wild-type mice that exhibit an increase in these cells
• at 20 weeks, iIELs are decreased compared to in wild-type mice
• at 10 and 20 weeks, mice exhibit decreased gamma-delta intestinal intraepithelial lymphocytes, which continue to decrease in number with age, compared with wild-type mice
• at 10 weeks, the number of CD4+CD8- alpha-beta intestinal intraepithelial lymphocytes is increased 7-fold compared to in wild-type mice
• NK cells stimulated with ligands to or antibodies against NK1.1, CD16, Ly49H, Ly49D, and NKG2D exhibit reduced cytokine secretion compared with similarly treated wild-type cells
• however, NK cell cytotoxicity in response to ITAM receptor stimulation is normal
• intestinal intraepithelial lymphocytes exhibit impaired cytolytic activities compared with wild-type cells

hematopoietic system
• intestinal intraepithelial lymphocytes (iIELs) exhibit increased spontaneous apoptosis compared to in wild-type mice
• gamma-delta iIELs are more susceptible to induction of apoptosis compared with alpha-beta iIELs
• intestinal intraepithelial lymphocytes (iIELs) is impaired
• however, extrathymic development of iIELs is normal in reconstitution experiments
• intestinal intraepithelial lymphocytes (iIELs) are slightly larger than wild-type cells
• in reconstitution experiments, intrathymic development of iIELs is impaired
• however, extrathymic development of iIELs is normal in reconstitution experiments
• at 10 weeks, the number of intestinal intraepithelial lymphocytes (iIELs) is increased 1.5- to 2-fold compared to in wild-type mice
• at 10 weeks, the number of CD4+CD8- alpha-beta iIELs is increased 7-fold compared to in wild-type mice
• the number of iIELs decrease over time unlike in wild-type mice that exhibit an increase in these cells
• at 20 weeks, iIELs are decreased compared to in wild-type mice
• at 10 and 20 weeks, mice exhibit decreased gamma-delta intestinal intraepithelial lymphocytes, which continue to decrease in number with age, compared with wild-type mice
• at 10 weeks, the number of CD4+CD8- alpha-beta intestinal intraepithelial lymphocytes is increased 7-fold compared to in wild-type mice
• NK cells stimulated with ligands to or antibodies against NK1.1, CD16, Ly49H, Ly49D, and NKG2D exhibit reduced cytokine secretion compared with similarly treated wild-type cells
• however, NK cell cytotoxicity in response to ITAM receptor stimulation is normal
• intestinal intraepithelial lymphocytes exhibit impaired cytolytic activities compared with wild-type cells

cellular
• intestinal intraepithelial lymphocytes (iIELs) exhibit increased spontaneous apoptosis compared to in wild-type mice
• gamma-delta iIELs are more susceptible to induction of apoptosis compared with alpha-beta iIELs


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
01/06/2026
MGI 6.24
The Jackson Laboratory