About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cux2tm1.1(cre)Mull
targeted mutation 1.1, Ulrich Mueller
MGI:5014209
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Mllt11tm1c(KOMP)Mbp/Mllt11tm1c(KOMP)Mbp
Cux2tm1.1(cre)Mull/Cux2+
involves: C57BL/6 * C57BL/6J * C57BL/6N MGI:7448861
cn2
Mllt11tm1c(KOMP)Mbp/Mllt11tm1c(KOMP)Mbp
Gt(ROSA)26Sortm9(CAG-tdTomato)Hze/Gt(ROSA)26Sor+
Cux2tm1.1(cre)Mull/Cux2+
involves: C57BL/6 * C57BL/6J * C57BL/6N MGI:7448866


Genotype
MGI:7448861
cn1
Allelic
Composition
Mllt11tm1c(KOMP)Mbp/Mllt11tm1c(KOMP)Mbp
Cux2tm1.1(cre)Mull/Cux2+
Genetic
Background
involves: C57BL/6 * C57BL/6J * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cux2tm1.1(cre)Mull mutation (1 available); any Cux2 mutation (43 available)
Mllt11tm1c(KOMP)Mbp mutation (0 available); any Mllt11 mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• apical shift in migrating CPNs is less pronounced when CPNs are labeled with EdU at E16
• EdU birthdating revealed impaired migration of upper layer (UL) cortical projection neurons (CPNs) into the cortical plate
• CPNs labeled with EdU at E14 show an apical shift of ~100 um at E18.5; a larger proportion of E14-born UL CPNs remain restricted to the deeper cortex bins
• however, no defects in the formation of Reelin+ CR cells nor in radial glial scaffolding are observed
• neurofilament (NF+) fiber staining showed a significant decrease in the thickness of cortical white matter tracts at E16.5 and E18.5
• neurofilament (NF+) fiber staining is significantly reduced in the corpus callosum at E18.5, reflecting a severe reduction in crossing callosal fibers
• DiI labeling of axonal projections is undetectable in the corpus callosum at E18.5, indicating impaired development of callosal projections
• in contrast, corticothalamic projections of the internal capsule remain unaffected
• coronal sections of the corpus callosum labeled with acetylated alpha-tubulin and Tubb3 showed decreased corpus callosum thickness at E18.5
• formation of UL CPNs is perturbed with progressively decreased numbers of Satb2+ cells in the upper bins from E16.5 to E18.5
• at E18.5, an increased proportion of DAPI+ nuclei are localized apically, towards the ventricular zone (VZ), relative to controls
• fewer Tbr2+ intermediate (basal) progenitors, which give rise to UL 2/3 CPNs, are found within deep regions at E18.5, suggesting altered formation and/or migration of nascent neurons from the subventricular zone (SVZ)
• marker analysis of UL CPNs showed decreased Satb2+ cell numbers and an apical shift of Satb2 expression starting at E16.5 and increasing in severity by E18.5; similarly, CDP/Cux1+ cell numbers are normal at E14.5 but start to decrease at E16.5 and are severely reduced at E18.5
• analysis of deep layer (DL) markers showed an apical shift in the expression domains of both Tbr1 (DL6-specific) and Ctip2 (DL5-specific) from E16.5 to E18.5, consistent with reduced cortical thickness and impaired UL formation
• at E18.5, thinning of the cortex is noted in the cortical plate and white matter below it
• cortex thinning is first noted at E16.5, increasing in severity by E18.5
• no thinning is seen at E14.5 when UL CPNs are born
• no increase in apoptosis is noted in cortical slices at E14.5 or E18.5
• at P28, Golgi-stained cortices show a severe reduction in total neurite outgrowth (length) and decreased branching complexity in mature UL2/3 CPNs in the cortex
• at P28, Golgi-stained UL CPNs show greatly attenuated dendritic arborization morphologies
• at P28, Golgi-stained UL2/3 CPNs show reduced dendritic branching complexity in the cortex; overall mature CPN morphology is much less complex with less elaborately branched neurites

cellular
• apical shift in migrating CPNs is less pronounced when CPNs are labeled with EdU at E16
• EdU birthdating revealed impaired migration of upper layer (UL) cortical projection neurons (CPNs) into the cortical plate
• CPNs labeled with EdU at E14 show an apical shift of ~100 um at E18.5; a larger proportion of E14-born UL CPNs remain restricted to the deeper cortex bins
• however, no defects in the formation of Reelin+ CR cells nor in radial glial scaffolding are observed




Genotype
MGI:7448866
cn2
Allelic
Composition
Mllt11tm1c(KOMP)Mbp/Mllt11tm1c(KOMP)Mbp
Gt(ROSA)26Sortm9(CAG-tdTomato)Hze/Gt(ROSA)26Sor+
Cux2tm1.1(cre)Mull/Cux2+
Genetic
Background
involves: C57BL/6 * C57BL/6J * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cux2tm1.1(cre)Mull mutation (1 available); any Cux2 mutation (43 available)
Gt(ROSA)26Sortm9(CAG-tdTomato)Hze mutation (4 available); any Gt(ROSA)26Sor mutation (944 available)
Mllt11tm1c(KOMP)Mbp mutation (0 available); any Mllt11 mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E18.5, cortices show an apical shift in the expression domain of Cux2, a marker of intermediate progenitors that give rise to upper layer (UL) 2/3 cortical projection neurons (CPNs)
• however, TdTomato levels are largely normal at E14.5, E16.5 and E18.5
• in culture, primary upper layer CPNs show a progressive reduction in neurite outgrowth and branching complexity





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
04/30/2024
MGI 6.23
The Jackson Laboratory