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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ncaphtm1.1Hiran
targeted mutation 1.1, Tatsuya Hirano
MGI:5703872
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Ncaphtm1.1Hiran/Ncaphtm1.2Hiran
Tg(Nes-cre)1Kln/0
involves: C57BL/6 * C57BL/6J * SJL MGI:5703887
cn2
Ncaphtm1.1Hiran/Ncaphtm1.2Hiran
Ncaph2tm1.1Hiran/Ncaph2tm1.2Hiran
Tg(Nes-cre)1Kln/0
involves: C57BL/6 * C57BL/6J * SJL MGI:5703890


Genotype
MGI:5703887
cn1
Allelic
Composition
Ncaphtm1.1Hiran/Ncaphtm1.2Hiran
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: C57BL/6 * C57BL/6J * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ncaphtm1.1Hiran mutation (1 available); any Ncaph mutation (30 available)
Ncaphtm1.2Hiran mutation (0 available); any Ncaph mutation (30 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• the frequencies of mitotic neural stem cells is increased, indicating that mitotic progression is slowed down
• E16.5 neural stem cells show an increase in the proportion of prometaphase and metaphase cells
• defects in mitotic chromosome architecture and segregation are less prominent than in mice conditionally deleted for Ncaph2

nervous system
• cerebral cortices are highly disorganized by E19.5
• some apoptosis is seen in the developing cortices at E13.5
• numbers of neural stem cells are decreased at E16.5
• numbers of neurons are decreased at E16.5
• neural stem cells undergo apoptosis in the ventricular zone at E16.5




Genotype
MGI:5703890
cn2
Allelic
Composition
Ncaphtm1.1Hiran/Ncaphtm1.2Hiran
Ncaph2tm1.1Hiran/Ncaph2tm1.2Hiran
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: C57BL/6 * C57BL/6J * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ncaph2tm1.1Hiran mutation (1 available); any Ncaph2 mutation (38 available)
Ncaph2tm1.2Hiran mutation (0 available); any Ncaph2 mutation (38 available)
Ncaphtm1.1Hiran mutation (1 available); any Ncaph mutation (30 available)
Ncaphtm1.2Hiran mutation (0 available); any Ncaph mutation (30 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• hyperclustering of chromocenters in neurons
• mice exhibit postmitotic cells with tail-like structures, indicative of defective chromosome segregation
• mitotic chromosomes are highly disorganized at prometaphase in 87.8% of cells
• cells with abnormal chromosomes progress through mitosis, exhibiting chromosome bridges in anaphase and dumbbell-shaped nucleus in subsequent G1 phase
• hyperclustering of chromocenters (the nuclear structure that forms from the association of pericentric heterochromatin from several different chromosomes during interphase) in neurons

nervous system
• cerebral cortices are disorganized at E16.5
• massive apoptosis in developing cortices at E13.5
• cerebral cortices are extremely thin at E16.5
• Sox2+ neural stem cells largely disappear
• neurons in the cortical plate are reduced at E16.5
• Brn2+ upper-layer (later born) neurons are depleted more severely than the Tbr1+ deep-layer (early born) neurons





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory