About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:3818443
Allelic
Composition
Cd247tm1Mhu/Cd247tm1Mhu
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cd247tm1Mhu mutation (0 available); any Cd247 mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• despite the reduction in T cell differentiation in the thymus, the numbers and ratios of CD4+ or CD8+ T cells in the spleen and lymph nodes, VDJ rearrangement, and the numbers and function of NK cells are normal
• intraepithelial lymphocytes fail to proliferate in response to stimulation with anti-CD3 antibodies and ConA unlike heterozygous cells
• TCR/CD3very low CD4+ and CD8+ single positive splenocytes fail to proliferate in response to anti-CD3 antibodies and ConA unlike heterozygous cells
• the size of the cortex is enlarged at the expense of the medulla
• the medulla is restricted to small regions unlike in heterozygous mice
• at 8 to 12 weeks, thymocyte number is decreased 5- to 10-fold compared to in heterozygous mice
• mice exhibit a delayed and reduced differentiation of double negative T cells into double positive TCR/CD3hi T cells in the thymus compared to in heterozygous mice instead generating TCR/CD3very low CD4+ and CD8+ single positive T cells
• however, intraepithelial lymphocytes express normal levels of TCR/CD3
• the percentage of double negative cells in the thymus is more than in heterozygous mice
• however, the absolute number of double negative cells is normal
• the percentage of double positive cells in the thymus is decreased compared to in heterozygotes
• the percentage of CD4+ single positive cells in the thymus is decreased compared to in heterozygous mice mice that are indistinguishable from wild-type mice
• the percentage of CD8+ single positive cells in the thymus is decreased compared to in heterozygous mice

hematopoietic system
• intraepithelial lymphocytes fail to proliferate in response to stimulation with anti-CD3 antibodies and ConA unlike heterozygous cells
• TCR/CD3very low CD4+ and CD8+ single positive splenocytes fail to proliferate in response to anti-CD3 antibodies and ConA unlike heterozygous cells
• the size of the cortex is enlarged at the expense of the medulla
• the medulla is restricted to small regions unlike in heterozygous mice
• at 8 to 12 weeks, thymocyte number is decreased 5- to 10-fold compared to in heterozygous mice
• mice exhibit a delayed and reduced differentiation of double negative T cells into double positive TCR/CD3hi T cells in the thymus compared to in heterozygous mice instead generating TCR/CD3very low CD4+ and CD8+ single positive T cells
• however, intraepithelial lymphocytes express normal levels of TCR/CD3
• the percentage of double negative cells in the thymus is more than in heterozygous mice
• however, the absolute number of double negative cells is normal
• the percentage of double positive cells in the thymus is decreased compared to in heterozygotes
• the percentage of CD4+ single positive cells in the thymus is decreased compared to in heterozygous mice mice that are indistinguishable from wild-type mice
• the percentage of CD8+ single positive cells in the thymus is decreased compared to in heterozygous mice

cellular
• intraepithelial lymphocytes fail to proliferate in response to stimulation with anti-CD3 antibodies and ConA unlike heterozygous cells
• TCR/CD3very low CD4+ and CD8+ single positive splenocytes fail to proliferate in response to anti-CD3 antibodies and ConA unlike heterozygous cells

endocrine/exocrine glands
• the size of the cortex is enlarged at the expense of the medulla
• the medulla is restricted to small regions unlike in heterozygous mice
• at 8 to 12 weeks, thymocyte number is decreased 5- to 10-fold compared to in heterozygous mice

growth/size/body


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
05/26/2026
MGI 6.24
The Jackson Laboratory