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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Emx1-cre)#Ito
transgene insertion, Shigeyoshi Itohara
MGI:5433170
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Cdkl5tm1.1Cogr/Cdkl5+
Tg(Emx1-cre)#Ito/0
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * C57BL/6J MGI:5574070
cn2
Cdkl5tm1.1Cogr/Y
Tg(Emx1-cre)#Ito/0
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * C57BL/6J MGI:5574071
cn3
Fezf2tm1.1Nses/Fezf2tm1.1Nses
Tbr1tm1Jlr/Tbr1tm1Jlr
Tg(Emx1-cre)#Ito/0
Tg(Mbp-MAPT/EGFP)#Eja/0
involves: 129S1/Sv * C57BL/6 MGI:5433181
cn4
Fezf2tm1.1Nses/Fezf2tm1.1Nses
Tg(CAG-cat,-EGFP)39Miya/0
Tg(Emx1-cre)#Ito/0
involves: 129S1/Sv * C57BL/6 * C57BL/6NJcl * DBA/2NJcl MGI:5433180
cn5
Marchf5tm1.1Ygi/Marchf5tm1.1Ygi
Tg(Emx1-cre)#Ito/0
involves: C57BL/6 MGI:6406743
cn6
Agap3tm1Ygi/Agap3tm1Ygi
Tg(Emx1-cre)#Ito/0
involves: C57BL/6 MGI:6719550


Genotype
MGI:5574070
cn1
Allelic
Composition
Cdkl5tm1.1Cogr/Cdkl5+
Tg(Emx1-cre)#Ito/0
Genetic
Background
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkl5tm1.1Cogr mutation (1 available); any Cdkl5 mutation (19 available)
Tg(Emx1-cre)#Ito mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mice exhibit normal activity levels and a trend for decreased head tracking
• in some mice




Genotype
MGI:5574071
cn2
Allelic
Composition
Cdkl5tm1.1Cogr/Y
Tg(Emx1-cre)#Ito/0
Genetic
Background
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkl5tm1.1Cogr mutation (1 available); any Cdkl5 mutation (19 available)
Tg(Emx1-cre)#Ito mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mice exhibit normal activity levels and a trend for decreased head tracking
• in some mice




Genotype
MGI:5433181
cn3
Allelic
Composition
Fezf2tm1.1Nses/Fezf2tm1.1Nses
Tbr1tm1Jlr/Tbr1tm1Jlr
Tg(Emx1-cre)#Ito/0
Tg(Mbp-MAPT/EGFP)#Eja/0
Genetic
Background
involves: 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fezf2tm1.1Nses mutation (1 available); any Fezf2 mutation (49 available)
Tbr1tm1Jlr mutation (1 available); any Tbr1 mutation (38 available)
Tg(Emx1-cre)#Ito mutation (0 available)
Tg(Mbp-MAPT/EGFP)#Eja mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Aberrant L6 projections to the brainstem in the Tbr1tm1Jlr/Tbr1tm1Jlr mice require Fezf2

nervous system
N
• unlike Tbr1tm1Jlr homozygotes, mice lack retrograde labeling of L5 and L6 projection neurons




Genotype
MGI:5433180
cn4
Allelic
Composition
Fezf2tm1.1Nses/Fezf2tm1.1Nses
Tg(CAG-cat,-EGFP)39Miya/0
Tg(Emx1-cre)#Ito/0
Genetic
Background
involves: 129S1/Sv * C57BL/6 * C57BL/6NJcl * DBA/2NJcl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fezf2tm1.1Nses mutation (1 available); any Fezf2 mutation (49 available)
Tg(CAG-cat,-EGFP)39Miya mutation (1 available)
Tg(Emx1-cre)#Ito mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• mice lack corticospinal axons in the brainstem




Genotype
MGI:6406743
cn5
Allelic
Composition
Marchf5tm1.1Ygi/Marchf5tm1.1Ygi
Tg(Emx1-cre)#Ito/0
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Marchf5tm1.1Ygi mutation (0 available); any Marchf5 mutation (18 available)
Tg(Emx1-cre)#Ito mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice show reduced alternation in the Y-maze at P21 and 3 months, suggesting poor short-term memory
• however, mice show normal behavior in the elevated plus maze
• mice spend less time grooming at P21
• mice exhibit increased immobility time in the open field test at P21

cellular
• neuronal mitochondrial volume and branch number are reduced in the cell body of neurons
• mitochondrial abnormalities are seen with higher frequency in small mitochondria than large mitochondria
• cardiolipin is reduced in mitochondria isolated from brains, however no differences are seen for other phospholipids
• however, mitochondrial swelling is absent and enhanced autophagy or mitophagy is not seen
• neuronal mitochondria shows numerous dilated, swollen cristae
• neuronal mitochondria shows empty matrices
• small and simple structured mitochondria are dominant in neurons, while large branched mitochondria are scarcely detected
• small mitochondria are also seen in astrocytes
• level of oxidized proteins is enhanced in the hippocampus indicating enhanced oxidative stress in neurons

hematopoietic system
• mice show enhanced microglial activation in the cerebral cortex and hippocampus

homeostasis/metabolism
• nearly all cardiolipin species are reduced in the brain
• cardiolipin is reduced in mitochondria isolated from brains

immune system
• mice show enhanced microglial activation in the cerebral cortex and hippocampus

nervous system
• mice show enhanced microglial activation in the cerebral cortex and hippocampus
• mice show enhanced astrogliosis in the cerebral cortex and hippocampus
• treatment with a radical scavenger Edaravone attenuates astrogliosis
• increase in small mitochondria in neurons and loss of large and branched mitochondria
• neurons show reduced endoplasmic reticulum (ER)-mitochondria contact sites; reduction in both total area and the number of ER-mitochondria contact sites and the frequency of ER-mitochondria contact, indicating reduced ER tethering to mitochondria




Genotype
MGI:6719550
cn6
Allelic
Composition
Agap3tm1Ygi/Agap3tm1Ygi
Tg(Emx1-cre)#Ito/0
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Agap3tm1Ygi mutation (0 available); any Agap3 mutation (38 available)
Tg(Emx1-cre)#Ito mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• immature dentate gyrus with decreased mature neuron numbers
• decreased mature neurons in the dentate gyrus

behavior/neurological
• at P21 and 8 weeks without increased anxiety





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory