About   Help   FAQ
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





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