About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:2174969
Allelic
Composition
Mapttm1Noh/Mapttm1Noh
Genetic
Background
involves: 129S4/SvJae
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mapttm1Noh mutation (0 available); any Mapt mutation (430 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• abnormal cerebellar parallel fiber axons; reduction in microtubule (MT) number and density and reduction in frequency of cross-bridges between MTs
• mice exhibit no other obvious abnormalities

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
NOT Alzheimer's disease DOID:10652 J:19030


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
12/10/2024
MGI 6.24
The Jackson Laboratory