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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rab13tm1.1Ktg
targeted mutation 1.1 Koko Katagiri
MGI:6151445
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rab13tm1.1Ktg/Rab13tm1.1Ktg involves: C57BL/6 MGI:7488604


Genotype
MGI:7488604
hm1
Allelic
Composition
Rab13tm1.1Ktg/Rab13tm1.1Ktg
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab13tm1.1Ktg mutation (0 available); any Rab13 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• at 6 to 8 weeks of age, mice show no differences in the ratio of naive T cells relative to control-mice
• in response to CCL21 exposure, the displacement and velocity of primary T cells during migration on ICAM-1 are reduced to 43% and 58% of those in control T cells, respectively
• in transwell migration assays, the numbers of T cells that migrate to the lower chambers containing CCL21 are markedly lower than those of control T cells; the numbers of T cells that migrate through ICAM-1-coated filters is not reduced relative to the number of T cells that migrate through uncoated filters, unlike in control cells
• in response to CCL21 exposure, primary T cells show a significant reduction in the shear stressresistant adhesion to ICAM-1 relative to control T cells
• analysis of the homing capability of adoptively transferred T cells showed that the extent of T cell trafficking into the spleen and peripheral lymph nodes is reduced to ~50% and 30%, respectively, of that in control cells
• spleen and peripheral lymph nodes show significantly lower numbers of T cells and B cells than control lymphoid tissues due to impaired lymphocyte trafficking
• however, numbers of T cells and B cells are normal in blood
• spleen is significantly smaller than in control mice
• upon stimulation with chemokine CCL21, Mst1 does not translocate to the leading edge but remains diffusely distributed in the cytoplasm of primary T cells, unlike in control T cells
• most CCL21-stimulated T cells show impaired redistribution of LFA-1, whereas ~30% of CCL21-treated control T cells display polarized morphologies with a leading edge and uropod, to which LFA-1 and CD44 are clustered, respectively
• however, the abundance of CCR7 (the receptor for CCL21) in T cells is similar to that in control T cells
• inguinal lymph nodes are significantly smaller than in control mice
• spleen and peripheral lymph nodes show significantly lower numbers of T cells and B cells than control lymphoid tissues

hematopoietic system
• in response to CCL21 exposure, the displacement and velocity of primary T cells during migration on ICAM-1 are reduced to 43% and 58% of those in control T cells, respectively
• in transwell migration assays, the numbers of T cells that migrate to the lower chambers containing CCL21 are markedly lower than those of control T cells; the numbers of T cells that migrate through ICAM-1-coated filters is not reduced relative to the number of T cells that migrate through uncoated filters, unlike in control cells
• in response to CCL21 exposure, primary T cells show a significant reduction in the shear stressresistant adhesion to ICAM-1 relative to control T cells
• analysis of the homing capability of adoptively transferred T cells showed that the extent of T cell trafficking into the spleen and peripheral lymph nodes is reduced to ~50% and 30%, respectively, of that in control cells
• spleen and peripheral lymph nodes show significantly lower numbers of T cells and B cells than control lymphoid tissues due to impaired lymphocyte trafficking
• however, numbers of T cells and B cells are normal in blood
• spleen is significantly smaller than in control mice
• upon stimulation with chemokine CCL21, Mst1 does not translocate to the leading edge but remains diffusely distributed in the cytoplasm of primary T cells, unlike in control T cells
• most CCL21-stimulated T cells show impaired redistribution of LFA-1, whereas ~30% of CCL21-treated control T cells display polarized morphologies with a leading edge and uropod, to which LFA-1 and CD44 are clustered, respectively
• however, the abundance of CCR7 (the receptor for CCL21) in T cells is similar to that in control T cells

cellular
• in response to CCL21 exposure, the displacement and velocity of primary T cells during migration on ICAM-1 are reduced to 43% and 58% of those in control T cells, respectively
• in transwell migration assays, the numbers of T cells that migrate to the lower chambers containing CCL21 are markedly lower than those of control T cells; the numbers of T cells that migrate through ICAM-1-coated filters is not reduced relative to the number of T cells that migrate through uncoated filters, unlike in control cells
• in response to CCL21 exposure, primary T cells show a significant reduction in the shear stressresistant adhesion to ICAM-1 relative to control T cells
• analysis of the homing capability of adoptively transferred T cells showed that the extent of T cell trafficking into the spleen and peripheral lymph nodes is reduced to ~50% and 30%, respectively, of that in control cells

mortality/aging
N
• mice are born with the expected Mendelian frequencies and grow normally

growth/size/body
N
• mice grow normally





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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory