About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nbntm2.1Zqw
targeted mutation 2.1, Zhao-Qi Wang
MGI:3578646
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Nbntm2Zqw/Nbntm2.1Zqw
Tg(Nes-cre)1Wme/0
involves: 129P2/OlaHsd * C57BL/6 * CBA MGI:3579666


Genotype
MGI:3579666
cn1
Allelic
Composition
Nbntm2Zqw/Nbntm2.1Zqw
Tg(Nes-cre)1Wme/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nbntm2.1Zqw mutation (0 available); any Nbn mutation (59 available)
Nbntm2Zqw mutation (0 available); any Nbn mutation (59 available)
Tg(Nes-cre)1Wme mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• neural stem and progenitor cells from E13.5 brains produce fewer and smaller neurospheres in culture, do not produce secondary neurospheres, and have an increased number of chromosomal breaks per metaphase; however, no increase in apoptosis is seen
• no primary neurospheres were isolated from newborn mutants
• at E15.5, E18.5, and P7, proliferation of cells is decreased in the outer external granule cell layer
• at E15.5, E18.5, and P7, apoptosis is increased in the inner external granule cell layer
• seen at P7
• at P0 the Purkinje cell layer is disorganized
• at P0 the granule cell layer is disorganized with a reduction in the number of granule cells and ectopic presence of Purkinje cells
• seen at P7-P21
• at P0 the Bergmann glia are abnormal

behavior/neurological
• when suspended by the tail mutants stretch out their hind limbs
• seen after P7
• cerebellar ataxia seen after P7
• after P7 mutants are unable to complete the balance beam test
• seen after P7
• seen after P7
• increased repetitive movements seen after P7

growth/size/body
• detected by P7 and mutants reach only about half of the body weight of control mice at weaning

cellular
• neural stem and progenitor cells from E13.5 brains produce fewer and smaller neurospheres in culture, do not produce secondary neurospheres, and have an increased number of chromosomal breaks per metaphase; however, no increase in apoptosis is seen
• no primary neurospheres were isolated from newborn mutants





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
10/29/2024
MGI 6.24
The Jackson Laboratory