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Phenotypes Associated with This Genotype
Genotype
MGI:3713120
Allelic
Composition
Atg5tm1Nmz/Atg5tm1Nmz
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atg5tm1Nmz mutation (1 available); any Atg5 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

absence of otoconia (right) or the presence of giant and abnormally shaped otoconial crystals (middle) in the utricle of Atg4bGt(A029E06)Wrst/Atg4bGt(A029E06)Wrst mice

nervous system
• neonates have ubiquitin-positive inclusions in a subset of neurons in the pons, dorsal root ganglia, spinal cord, hypothalamus, midbrain and trigeminal ganglia
• inclusions are found in the anterior lobe of the pituitary
• neonates have ubiquitin-positive inclusions in a subset of neurons in the pons, dorsal root ganglia, spinal cord, hypothalamus, midbrain and trigeminal ganglia
• inclusions are time-dependent and are more limited in newborns than in adults

hearing/vestibular/ear
• mice exhibit an accumulation of eosinophilic globular substance in the utricle unlike in wild-type mice
• in some mice
• in some mice

liver/biliary system
• inclusions are found in the liver
• neonates have ubiquitin-positive inclusions in hepatocytes

endocrine/exocrine glands
• inclusions are found in the adrenal gland
• inclusions are found in the anterior lobe of the pituitary


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
01/28/2026
MGI 6.24
The Jackson Laboratory