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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Atp2b2wri
wriggle
MGI:1857092
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Atp2b2wri/Atp2b2wri involves: BALB/cAnN MGI:3694741
ht2
Atp2b2wri/Atp2b2+ involves: BALB/cAnN MGI:3694744


Genotype
MGI:3694741
hm1
Allelic
Composition
Atp2b2wri/Atp2b2wri
Genetic
Background
involves: BALB/cAnN
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atp2b2wri mutation (1 available); any Atp2b2 mutation (66 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• starting at 10 days after birth, can not maintain upright posture
• choreoathetosis movement associated with the dystonic posture
• starting at 10 days after birth

nervous system
• impaired development of the dendritic trees of the Purkinje cells
• patchy loss of outer hair cells at 3 months of age
• almost complete loss of the outer hair cells by 6 months of age
• decreased synaptic connections of parallel fibers on the dendritic spines of the Purkinje cells as early as 2 weeks after birth
• decrease in the number of spiral ganglion cells observed starting at 3 months of age
• most spiral ganglion cells are lost throughout the turns by 6 months of age

hearing/vestibular/ear
• patchy loss of outer hair cells at 3 months of age
• almost complete loss of the outer hair cells by 6 months of age
• the cochlea degenerate severely within three months after birth
• the sensory epithelium of the saccule became atrophic at 3 months of age
• the saccule degenerate severely within three months after birth
• no wave which can be regarded as wave I to VI in ABR audiometry at any age
• at maximum stimulation of 110 dBSPL, a low amplitude of wave after a short latency was observed
• no waves below 100 dBSPL
• severe hearing loss is apparent from early after birth (J:56737)

cellular
• impaired development of the dendritic trees of the Purkinje cells




Genotype
MGI:3694744
ht2
Allelic
Composition
Atp2b2wri/Atp2b2+
Genetic
Background
involves: BALB/cAnN
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atp2b2wri mutation (1 available); any Atp2b2 mutation (66 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• the cochlea degeneration is noted (J:56737)
• the saccule remains intact (J:56737)
• at 3 month (J:71283)
• mild hearing loss is present in mice less than one month old
• progresses to severe hearing loss after one month

nervous system
• decrease in the number of spiral ganglion cells observed by 6 months of age





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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
12/10/2024
MGI 6.24
The Jackson Laboratory