About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mogtm1(cre)Gkl
targeted mutation 1, George Kollias
MGI:3689957
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Gt(ROSA)26Sortm1(HA)Libl/Gt(ROSA)26Sortm1(HA)Libl
Mogtm1(cre)Gkl/?
Tg(TcraCl4,TcrbCl4)1Shrm/0
involves: 129/Sv * BALB/c * C57BL/6 MGI:3805339
cn2
Gt(ROSA)26Sortm1(HA)Libl/Gt(ROSA)26Sortm1(HA)Libl
Mogtm1(cre)Gkl/?
involves: 129/Sv * C57BL/6 MGI:3805338
cn3
Fastm1Cgn/Fastm1Cgn
Mogtm1(cre)Gkl/Mog+
Tnfrsf1atm1Mak/Tnfrsf1atm1Mak
involves: 129S2/SvPas * C57BL/6 MGI:3690542
cn4
Fastm1Cgn/Fastm1Cgn
Mogtm1(cre)Gkl/Mog+
involves: C57BL/6 MGI:3690541
cn5
Gt(ROSA)26Sortm1(HBEGF)Awai/Gt(ROSA)26Sortm1(HBEGF)Awai
Mogtm1(cre)Gkl/?
involves: C57BL/6 MGI:3772815
cn6
Faddtm1Mpa/Faddtm1Mpa
Mogtm1(cre)Gkl/Mog+
involves: C57BL/6 * SJL MGI:4880724
cx7
Mogtm1(cre)Gkl/Mogtm1(cre)Gkl
Tg(Tcra2D2,Tcrb2D2)1Kuch/0
C57BL/6-Mogtm1(cre)Gkl Tg(Tcra2D2,Tcrb2D2)1Kuch MGI:4461061


Genotype
MGI:3805339
cn1
Allelic
Composition
Gt(ROSA)26Sortm1(HA)Libl/Gt(ROSA)26Sortm1(HA)Libl
Mogtm1(cre)Gkl/?
Tg(TcraCl4,TcrbCl4)1Shrm/0
Genetic
Background
involves: 129/Sv * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1(HA)Libl mutation (0 available); any Gt(ROSA)26Sor mutation (993 available)
Mogtm1(cre)Gkl mutation (1 available); any Mog mutation (58 available)
Tg(TcraCl4,TcrbCl4)1Shrm mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• 4 weeks after receiving transfer of HA-specific effector CD8 T cells, mice exhibit weight loss

behavior/neurological
• 4 weeks after receiving transfer of HA-specific effector CD8 T cells, severely affected animals display difficulty to right themselves when overturned
• 4 weeks after receiving transfer of HA-specific effector CD8 T cells (Tc1 cells), severely affected animals exhibit tremors
• 4 weeks after receiving transfer of HA-specific effector CD8 T cells, severely affected animals show reduced mobility

nervous system
• inflammation is also observed frequently in cerebellum, fornix and periventricular areas
• by 5 days following transfer of Tc1 cells, all mutants examined show spinal cord inflammation
• T cell infiltration into spinal cord starts on day 5 after transfer and peaks at day 28
• by 5 days following transfer of Tc1 cells, all mutants examined show optic nerve inflammation
• apoptosis in optic nerve and spinal cord is seen at early time points following Tc1 transfer
• focal areas with reduced myelin density and thin myelin sheaths are observed in animals after transfer of Tc1 cells
• vacuolization is seen at day 5 after Tc1 cell transfer
• by 5 days following transfer of Tc1 cells, demyelination is observed in the spinal cord and optic nerve
• from 9 days post-transfer, most mutants exhibit extensive demyelination in optic nerves
• by day 19, actively demyelinating lesions show severe axonal damage

vision/eye
• focal areas with reduced myelin density and thin myelin sheaths are observed in animals after transfer of Tc1 cells
• vacuolization is seen at day 5 after Tc1 cell transfer

immune system
• inflammation is also observed frequently in cerebellum, fornix and periventricular areas
• by 5 days following transfer of Tc1 cells, all mutants examined show spinal cord inflammation
• T cell infiltration into spinal cord starts on day 5 after transfer and peaks at day 28
• by 5 days following transfer of Tc1 cells, all mutants examined show optic nerve inflammation




Genotype
MGI:3805338
cn2
Allelic
Composition
Gt(ROSA)26Sortm1(HA)Libl/Gt(ROSA)26Sortm1(HA)Libl
Mogtm1(cre)Gkl/?
Genetic
Background
involves: 129/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1(HA)Libl mutation (0 available); any Gt(ROSA)26Sor mutation (993 available)
Mogtm1(cre)Gkl mutation (1 available); any Mog mutation (58 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mutants do not show neurological signs when followed for up to 9 months of age

immune system
N
• no deletion of HA-specific CD8 T cells is observed




Genotype
MGI:3690542
cn3
Allelic
Composition
Fastm1Cgn/Fastm1Cgn
Mogtm1(cre)Gkl/Mog+
Tnfrsf1atm1Mak/Tnfrsf1atm1Mak
Genetic
Background
involves: 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fastm1Cgn mutation (1 available); any Fas mutation (82 available)
Mogtm1(cre)Gkl mutation (1 available); any Mog mutation (58 available)
Tnfrsf1atm1Mak mutation (2 available); any Tnfrsf1a mutation (52 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• B and T cell distribution in the lymph nodes is normal
• the fraction of B220+ T cells in the lymph nodes and the thymic distribution of CD4/CD8 cells are similar to wild-type
• mice are almost completely resistant to induction of experimental autoimmune encephalomyelitis (EAE) by injection of MOG p35-55
• almost no oligodendrocyte apoptosis after EAE induction unlike in wild-type mice
• reduction in demyelination and inflammation after induction of EAE is greater than in mutant mice wild-type for Tnfrsf1a
• 24 days after induction of EAE, minimal axonal injury is seen in spinal cords




Genotype
MGI:3690541
cn4
Allelic
Composition
Fastm1Cgn/Fastm1Cgn
Mogtm1(cre)Gkl/Mog+
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fastm1Cgn mutation (1 available); any Fas mutation (82 available)
Mogtm1(cre)Gkl mutation (1 available); any Mog mutation (58 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• the fraction of B220+ T cells in the lymph nodes and the thymic distribution of CD4/CD8 cells are similar to wild-type
• reduction in the onset and severity, but not incidence, of experimental autoimmune encephalomyelitis (EAE) induced by injection of MOG p35-55
• demyelination induced by injection of MOG p35-55 is reduced by about 70% compared to wild-type
• perivascular and parenchymal infiltration by T lymphocytes and macrophages is also reduced after induction of EAE
• mild reduction in oligodendrocyte apoptosis after EAE induction




Genotype
MGI:3772815
cn5
Allelic
Composition
Gt(ROSA)26Sortm1(HBEGF)Awai/Gt(ROSA)26Sortm1(HBEGF)Awai
Mogtm1(cre)Gkl/?
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1(HBEGF)Awai mutation (4 available); any Gt(ROSA)26Sor mutation (993 available)
Mogtm1(cre)Gkl mutation (1 available); any Mog mutation (58 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• after intaperitoneal injection with diptheria toxin 3 times daily for 7 days, mice present with weight loss after ~30 days

behavior/neurological
• after intaperitoneal injection with diptheria toxin 3 times daily for 7 days, mice present with tremor after ~30 days
• after intaperitoneal injection with diptheria toxin 3 times daily for 7 days, mice present with hindlimb paralysis after ~30 days

nervous system
• 3 days following diptheria toxin injection 3 times daily for 7 days, substantial apoptosis is detected in the granular layer of the cerebella of double mutants; cells are likely oligodendrocytes, but may be granule cells
• reactive astrogliosis is observed, as well as inflammatory cells, in oligodendrocytes after diptheria toxin injection 3 times daily for 7 days
• after intaperitoneal injection with diptheria toxin 3 times daily for 7 days, severe destruction of myelinated structures throughout the CNS is observed
• diptheria toxin-induced demyelination is observed in treated double mutants

immune system
• after diptheria toxin treatment for 7 days, low titers of IgM diptheria toxin-specific antibodies are detected in the serum; DT-specific IgG1 antibodies are detected later, and amounts are ~50-fold lower than in a typical hapten-induced antiboby response

cellular
• 3 days following diptheria toxin injection 3 times daily for 7 days, substantial apoptosis is detected in the granular layer of the cerebella of double mutants; cells are likely oligodendrocytes, but may be granule cells




Genotype
MGI:4880724
cn6
Allelic
Composition
Faddtm1Mpa/Faddtm1Mpa
Mogtm1(cre)Gkl/Mog+
Genetic
Background
involves: C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Faddtm1Mpa mutation (0 available); any Fadd mutation (18 available)
Mogtm1(cre)Gkl mutation (1 available); any Mog mutation (58 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• peripheral T cell activation is normal
• MOG35-55-treated mice exhibit less severe disease and reduced oligodendrocyte apoptosis compared with similarly treated wild-type mice
• however, MOG35-55-treated mice exhibit normal T cell activation

nervous system
N
• mice exhibit normal myelination
• oligodendrocytes are completely resistant to TNF-induced apoptosis unlike wild-type mice
• MOG35-55-treated mice exhibit less oligodendrocyte apoptosis compared to in similarly treated wild-type mice

cellular
• oligodendrocytes are completely resistant to TNF-induced apoptosis unlike wild-type mice
• MOG35-55-treated mice exhibit less oligodendrocyte apoptosis compared to in similarly treated wild-type mice




Genotype
MGI:4461061
cx7
Allelic
Composition
Mogtm1(cre)Gkl/Mogtm1(cre)Gkl
Tg(Tcra2D2,Tcrb2D2)1Kuch/0
Genetic
Background
C57BL/6-Mogtm1(cre)Gkl Tg(Tcra2D2,Tcrb2D2)1Kuch
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mogtm1(cre)Gkl mutation (1 available); any Mog mutation (58 available)
Tg(Tcra2D2,Tcrb2D2)1Kuch mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• between 15% and 20% of mice develop spontaneous EAE

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
multiple sclerosis DOID:2377 OMIM:612594
OMIM:612595
OMIM:612596
J:151335





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
11/12/2024
MGI 6.24
The Jackson Laboratory