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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ndel1tm1.1Shr
targeted mutation 1.1, Shinji Hirotsune
MGI:3589465
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ndel1tm1.1Shr/Ndel1tm1.1Shr involves: 129S6/SvEvTac MGI:3589747
ht2
Ndel1tm1.1Shr/Ndel1tm2Shr involves: 129S6/SvEvTac MGI:3589750
cx3
Pafah1b1tm1Awb/Pafah1b1+
Ndel1tm1.1Shr/Ndel1+
involves: 129S6/SvEvTac MGI:3589752
cx4
Pafah1b1tm2.2Awb/Pafah1b1+
Ndel1tm1.1Shr/Ndel1+
involves: 129S6/SvEvTac MGI:3589751


Genotype
MGI:3589747
hm1
Allelic
Composition
Ndel1tm1.1Shr/Ndel1tm1.1Shr
Genetic
Background
involves: 129S6/SvEvTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ndel1tm1.1Shr mutation (0 available); any Ndel1 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygous embryos are present at E3.5 but absent at E5.5

embryo
• in blastocyst cultures the inner cell mass grows poorly and degenerates shortly after 3 days in culture




Genotype
MGI:3589750
ht2
Allelic
Composition
Ndel1tm1.1Shr/Ndel1tm2Shr
Genetic
Background
involves: 129S6/SvEvTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ndel1tm1.1Shr mutation (0 available); any Ndel1 mutation (40 available)
Ndel1tm2Shr mutation (1 available); any Ndel1 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• dendritic extensions of postmiotic neurons in the cortical plate are irregular and fragmented
• mild partial splitting and diffuse pyramidal cells are seen in the CA3 and CA2 regions of the hippocampus




Genotype
MGI:3589752
cx3
Allelic
Composition
Pafah1b1tm1Awb/Pafah1b1+
Ndel1tm1.1Shr/Ndel1+
Genetic
Background
involves: 129S6/SvEvTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ndel1tm1.1Shr mutation (0 available); any Ndel1 mutation (40 available)
Pafah1b1tm1Awb mutation (0 available); any Pafah1b1 mutation (160 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E15.5, but not at E11.5, increased apoptosis is seen in the ventricular zone
• migration defects in the hippocampus are slightly more severe than in Pafah1b1 single heterozygotes with the number of cells the reached layer II now reduced
• dendritic extensions of postmiotic neurons in the cortical plate are irregular and fragmented
• a mild reduction in the number of cells in the neocortex is seen with preferential loss of later migrating cells

cellular
• at E15.5, but not at E11.5, increased apoptosis is seen in the ventricular zone
• migration defects in the hippocampus are slightly more severe than in Pafah1b1 single heterozygotes with the number of cells the reached layer II now reduced




Genotype
MGI:3589751
cx4
Allelic
Composition
Pafah1b1tm2.2Awb/Pafah1b1+
Ndel1tm1.1Shr/Ndel1+
Genetic
Background
involves: 129S6/SvEvTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ndel1tm1.1Shr mutation (0 available); any Ndel1 mutation (40 available)
Pafah1b1tm2.2Awb mutation (0 available); any Pafah1b1 mutation (160 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• dendritic extensions of postmiotic neurons in the cortical plate are irregular and fragmented
• partial splitting of the pyramidal cells in the CA3 regions of the hippocampus is seen unlike in either single heterozygote





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory