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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Atp9aem1Bcgen
endonuclease-mediated mutation 1, Biocytogen LLC
MGI:7580494
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Atp9aem1Bcgen/Atp9aem1Bcgen involves: C57BL/6 MGI:7610011


Genotype
MGI:7610011
hm1
Allelic
Composition
Atp9aem1Bcgen/Atp9aem1Bcgen
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atp9aem1Bcgen mutation (0 available); any Atp9a mutation (79 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• median survival is 252.5 days, much lower than the 627 days in wild-type mice

behavior/neurological
• in the Morris Water Maze, mice take more time and longer distances to find the invisible platform on day 2 and/or day 5 and mice cross the distant platform area less frequency and spend less time in the target quadrant during spatial probe testing on day 6, indicating disrupted hippocampus-depended spatial learning and memory
• in the Morris Water Maze, mice take more time and longer distances to find the invisible platform on day 2 and/or day 5 and mice cross the distant platform area less frequency and spend less time in the target quadrant during spatial probe testing on day 6, indicating disrupted hippocampus-depended spatial learning and memory
• the grasping score in the coat hanger test and latency to fall in the wire hang test are reduced, indicating impaired muscle strength
• in the open field, mice exhibit higher crossing frequency and residence time in the central area and higher total movement distance and mean velocity, indicating hyperactivity
• mice exhibit an increase in total number of arm entries, movement distance, and mean velocity in the Y-maze test, indicating hyperactivity, however no changes in spontaneous alternations in the Y-maze test are seen
• in the elevated plus maze test, mice spend more time in the open arms and a greater willingness to move beyond the edges, show a greater total distance of movement and higher mean velocity, indicating hyperactivity but no effect on anxiety

nervous system
• mice have severely damaged neuronal neurite morphology
• the intersection numbers of dendritic arborizations in the motor cortex and hippocampus are reduced
• the total intersection number per neuron in the motor cortex shows a reduction compared to that in the hippocampus
• the density of secondary dendritic spines in the pyramidal neurons of the motor cortex is reduced
• mice show impaired synaptic transmission in the primary motor cortex and hippocampus
• however, synaptic transmission of pyramidal neurons in the secondary motor cortex is unaffected
• the frequency, but not amplitude, of miniature excitatory postsynaptic currents (mEPSCs) is reduced in the primary motor cortex
• both the frequency and amplitude of mEPSCs in hippocampal CA1 pyramidal neurons are decreased
• however, neither frequency or amplitude of mEPSCs is altered in M2 pyramidal neurons

reproductive system
• complete infertility is seen when homozygotes are mated
• only a small percentage of homozygotes are obtained by matings between homozygotes and heterozygotes; these surviving mice have no obvious differences in physical characteristics and no microcephaly is seen

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
specific developmental disorder DOID:0060038 J:335674





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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
11/12/2024
MGI 6.24
The Jackson Laboratory