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Phenotypes Associated with This Genotype
Genotype
MGI:8243876
Allelic
Composition
Anxa11em1Lcu/Anxa11+
Genetic
Background
C57BL/6J-Anxa11em1Lcu
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Anxa11em1Lcu mutation (0 available); any Anxa11 mutation (74 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• paralysis is not seen up to 12 months of age, although occasional hindlimb spasms are seen
• spasms are less frequent than in homozygous mice from 8-9 months onward

behavior/neurological
N
• mice exhibit intact working memory in the Y-maze and normal novelty discrimination
• mice at 10 months of age show anxiety-like behavior in the elevated plus maze, with fewer entries into the open arms
• mice show significant motor decline at 10 months of age
• onset and progression of disease is similar to that seen in homozygotes
• reduction in spontaneous locomotor activity

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
amyotrophic lateral sclerosis type 23 DOID:0080225 OMIM:617839
J:371245


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
08/05/2025
MGI 6.24
The Jackson Laboratory