About   Help   FAQ
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





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory