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Phenotypes Associated with This Genotype
Genotype
MGI:3771318
Allelic
Composition
Mapttm1(MAPT)Vln/Mapttm1(MAPT)Vln
Genetic
Background
FVB.Cg-Mapttm1(MAPT)Vln
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mapttm1(MAPT)Vln mutation (0 available); any Mapt mutation (428 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• a motor deficit on beam walk test in all mice by 9-12 moths
• impaired in rotarod performance by age 9-10 months
• homozygous mice are indistinguishable from wild-type mice until 6 months old
• no clasping of limbs

nervous system
N
• axonal dilations were completely absent in brain and spinal cord at any age
• reaction with thioflavin S or X-34 was completely absent confirming the total absence of tauopathy


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)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory