About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Lck-cre)#Nik
transgene insertion, Nigel Killeen
MGI:4819511
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Tbc1d10ctm1.1Psou/Tbc1d10ctm1.2Psou
Tg(Lck-cre)#Nik/0
involves: 129S2/SvPas * C57BL/6 * C57BL/6J * DBA/2 MGI:5578119
cn2
Rr7tm3.1Kio/Rr7+
Tg(Lck-cre)#Nik/0
involves: 129S4/SvJae * C57BL/6 * DBA/2 MGI:5305076
cn3
Myh9tm5Rsad/Myh9tm5Rsad
Tg(Lck-cre)#Nik/0
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * DBA/2 MGI:4838531


Genotype
MGI:5578119
cn1
Allelic
Composition
Tbc1d10ctm1.1Psou/Tbc1d10ctm1.2Psou
Tg(Lck-cre)#Nik/0
Genetic
Background
involves: 129S2/SvPas * C57BL/6 * C57BL/6J * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbc1d10ctm1.1Psou mutation (1 available); any Tbc1d10c mutation (19 available)
Tbc1d10ctm1.2Psou mutation (1 available); any Tbc1d10c mutation (19 available)
Tg(Lck-cre)#Nik mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• mice exhibit normal early antigen-specific B cell response




Genotype
MGI:5305076
cn2
Allelic
Composition
Rr7tm3.1Kio/Rr7+
Tg(Lck-cre)#Nik/0
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• unlike wild-type cells, a portion of peripheral CD4+ T cells expressing CD8
• however, the number of CD4+(CD8+) decreases with age compared with Rr7tm3.1Kio heterozygotes due to cre-mediated removal of the CD2 LCR

immune system
• unlike wild-type cells, a portion of peripheral CD4+ T cells expressing CD8
• however, the number of CD4+(CD8+) decreases with age compared with Rr7tm3.1Kio heterozygotes due to cre-mediated removal of the CD2 LCR




Genotype
MGI:4838531
cn3
Allelic
Composition
Myh9tm5Rsad/Myh9tm5Rsad
Tg(Lck-cre)#Nik/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myh9tm5Rsad mutation (1 available); any Myh9 mutation (219 available)
Tg(Lck-cre)#Nik mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• the frequency of naive T cells in contact with high-endothelial venules is increased compared to in wild-type mice
• in adoptive transfer experiments, T cells exhibit shorter tracks, less displacement from their origin, reduced median speed, lower frequency of cells reaching peak instantaneous velocities, increased median turning angle, decreased average motility coefficient, and greater accumulation in lymph nodes due to impaired lymph node exit compared with wild-type cells
• naive T cells exhibit reduced Transwell chemotaxis in response to CCL21 compared with wild-type cells
• naive T cells exhibit inefficient crawling within a confined environment (8-4 um) compared with wild-type cells
• however, T cell crawling in a large width (12-20 um) lane is normal
• T cells exhibit a 2-fold greater adhesion to ICAM-1 under flow compared with similarly treated wild-type cells
• naive T cells exhibit inefficient crawling within a confined environment (8-4 um) compared with wild-type cells
• however, T cell crawling in a large width (12-20 um) lane is normal
• in the periphery (lymph nodes and blood)
• however, thymic populations are normal
• the frequency of naive T cells in contact with high-endothelial venules is increased compared to in wild-type mice
• T cells exhibit a 2-fold greater adhesion to ICAM-1 under flow compared with similarly treated wild-type cells
• migration of T cells on Transwell membranes is reduced compared with wild-type cells
• in adoptive transfer experiments, T cells exhibit shorter tracks, less displacement from their origin, reduced median speed, lower frequency of cells reaching peak instantaneous velocities, increased median turning angle, decreased average motility coefficient, and greater accumulation in lymph nodes due to impaired lymph node exit compared with wild-type cells
• naive T cells exhibit reduced Transwell chemotaxis in response to CCL21 compared with wild-type cells
• naive T cells exhibit inefficient crawling within a confined environment compared with wild-type cells
• despite a reduction in number, the percentage of CD8+ T cells in the lymph nodes tends to increase compared to in wild-type mice
• despite a reduction in number, the percentage of CD8+ T cells in the lymph nodes tends to increase compared to in wild-type mice

hematopoietic system
• the frequency of naive T cells in contact with high-endothelial venules is increased compared to in wild-type mice
• in adoptive transfer experiments, T cells exhibit shorter tracks, less displacement from their origin, reduced median speed, lower frequency of cells reaching peak instantaneous velocities, increased median turning angle, decreased average motility coefficient, and greater accumulation in lymph nodes due to impaired lymph node exit compared with wild-type cells
• naive T cells exhibit reduced Transwell chemotaxis in response to CCL21 compared with wild-type cells
• naive T cells exhibit inefficient crawling within a confined environment (8-4 um) compared with wild-type cells
• however, T cell crawling in a large width (12-20 um) lane is normal
• T cells exhibit a 2-fold greater adhesion to ICAM-1 under flow compared with similarly treated wild-type cells
• naive T cells exhibit inefficient crawling within a confined environment (8-4 um) compared with wild-type cells
• however, T cell crawling in a large width (12-20 um) lane is normal
• in the periphery (lymph nodes and blood)
• however, thymic populations are normal
• the frequency of naive T cells in contact with high-endothelial venules is increased compared to in wild-type mice
• T cells exhibit a 2-fold greater adhesion to ICAM-1 under flow compared with similarly treated wild-type cells
• migration of T cells on Transwell membranes is reduced compared with wild-type cells
• in adoptive transfer experiments, T cells exhibit shorter tracks, less displacement from their origin, reduced median speed, lower frequency of cells reaching peak instantaneous velocities, increased median turning angle, decreased average motility coefficient, and greater accumulation in lymph nodes due to impaired lymph node exit compared with wild-type cells
• naive T cells exhibit reduced Transwell chemotaxis in response to CCL21 compared with wild-type cells
• naive T cells exhibit inefficient crawling within a confined environment compared with wild-type cells
• despite a reduction in number, the percentage of CD8+ T cells in the lymph nodes tends to increase compared to in wild-type mice

cellular
• the frequency of naive T cells in contact with high-endothelial venules is increased compared to in wild-type mice
• in adoptive transfer experiments, T cells exhibit shorter tracks, less displacement from their origin, reduced median speed, lower frequency of cells reaching peak instantaneous velocities, increased median turning angle, decreased average motility coefficient, and greater accumulation in lymph nodes due to impaired lymph node exit compared with wild-type cells
• naive T cells exhibit reduced Transwell chemotaxis in response to CCL21 compared with wild-type cells
• naive T cells exhibit inefficient crawling within a confined environment (8-4 um) compared with wild-type cells
• however, T cell crawling in a large width (12-20 um) lane is normal
• T cells exhibit a 2-fold greater adhesion to ICAM-1 under flow compared with similarly treated wild-type cells
• naive T cells exhibit inefficient crawling within a confined environment (8-4 um) compared with wild-type cells
• however, T cell crawling in a large width (12-20 um) lane is normal





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
04/23/2024
MGI 6.23
The Jackson Laboratory