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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pou4f3tm1Wagq
targeted mutation 1, Guoqiang Wan
MGI:8220018
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Pou4f3tm1Wagq/Pou4f3tm1Wagq involves: 129S6/SvEvTac * C57BL/6J MGI:8220065
hm2
Pou4f3tm1Wagq/Pou4f3tm1Wagq involves: 129S6/SvEvTac * C57BL/6J * FVB/N MGI:8220070
ht3
Pou4f3tm1Wagq/Pou4f3+ involves: 129S6/SvEvTac * C57BL/6J MGI:8220064
ht4
Pou4f3tm1Wagq/Pou4f3+ involves: 129S6/SvEvTac * C57BL/6J * FVB/N MGI:8220069


Genotype
MGI:8220065
hm1
Allelic
Composition
Pou4f3tm1Wagq/Pou4f3tm1Wagq
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pou4f3tm1Wagq mutation (0 available); any Pou4f3 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• loss of all hair cells within the first month of life
• extensive degeneration at P3
• profoundly deaf within the first month of life

nervous system
• loss of all hair cells within the first month of life
• extensive degeneration at P3




Genotype
MGI:8220070
hm2
Allelic
Composition
Pou4f3tm1Wagq/Pou4f3tm1Wagq
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pou4f3tm1Wagq mutation (0 available); any Pou4f3 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• profoundly deaf at 3 weeks of age




Genotype
MGI:8220064
ht3
Allelic
Composition
Pou4f3tm1Wagq/Pou4f3+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pou4f3tm1Wagq mutation (0 available); any Pou4f3 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
N
• rotarod tests indicate vestibular function is intact
• decreased mitochondrial density and mitochondrial vacuolization
• at 6 months of age stereociliary bundles are fused and elongated at both turns
• decreased mitochondrial density and mitochondrial vacuolization
• some outer hair cells are missing at the 32 kHz region
• many OHCs are lost in the middle-basal turn and replaced with filled flat epithelium in mice at 6 months of age
• remaining OHCs appear to have fewer steriocilia bundles at 6 months of age
• selective degeneration of outer but not inner hair cells at the 32 kHz region at 4-6 months of age
• utricular sensory epithelia appears smaller compared to wild-type controls
• reduced peak 1 amplitudes at 32 kHz at 2 months of age
• at 3 and 7 months of age P1 amplitudes are significantly and progressively altered from high to low cochlear frequencies
• at 3 and 7 months of age ABR thresholds are significantly and progressively altered from high to low cochlear frequencies
• at 3 and 7 months of age DPOAE thresholds are significantly and progressively altered from high to low cochlear frequencies
• adult onset, progressive hearing loss starting with high frequencies
• Background Sensitivity: hearing loss is earlier compared to mice crossed onto an FVB/N background
• treatment with 4-diethylaminobenzaldehyde (an aldehyde dehydrogenase inhibitor) protected hearing function during the treatment period

cellular
• decreased mitochondrial density and mitochondrial vacuolization in cochlear inner and outer hair cells

nervous system
• decreased mitochondrial density and mitochondrial vacuolization
• at 6 months of age stereociliary bundles are fused and elongated at both turns
• decreased mitochondrial density and mitochondrial vacuolization
• some outer hair cells are missing at the 32 kHz region
• many OHCs are lost in the middle-basal turn and replaced with filled flat epithelium in mice at 6 months of age
• remaining OHCs appear to have fewer steriocilia bundles at 6 months of age
• selective degeneration of outer but not inner hair cells at the 32 kHz region at 4-6 months of age

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
autosomal dominant nonsyndromic deafness 15 DOID:0110546 OMIM:602459
J:296699




Genotype
MGI:8220069
ht4
Allelic
Composition
Pou4f3tm1Wagq/Pou4f3+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pou4f3tm1Wagq mutation (0 available); any Pou4f3 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• significant loss of OHCs at 32 kHz at 12 months of age
• decrease in P1 amplitudes at most frequencies
• increased thresholds at high frequencies at 12 months of age
• increased thresholds at high frequencies at 12 months of age
• at 4 months of age exposure to acoustic trauma induced more severe hearing loss compared to similarly treated wild-type mice
• at 12 months of age
• Background Sensitivity: hearing loss is later compared to mice on a mixed 129S6/SvEvTac and C57BL/6J background

nervous system
• significant loss of OHCs at 32 kHz at 12 months of age





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last database update
03/18/2025
MGI 6.24
The Jackson Laboratory