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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Espnlem1Pgg
endonuclease-mediated mutation 1, Peter G Gillespie
MGI:7581062
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Espnlem1Pgg/Espnlem1Pgg Not Specified MGI:7610476
ht2
Espnlem1Pgg/Espnlem2Pgg Not Specified MGI:7610482


Genotype
MGI:7610476
hm1
Allelic
Composition
Espnlem1Pgg/Espnlem1Pgg
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Espnlem1Pgg mutation (1 available); any Espnl mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
N
• mice exhibit normal organization of utricle hair bundles in both striolar and extrastriolar regions and show no overt vestibular phenotype
• at P10.5 and P30.5, the shortest row (row 3) of stereocilia is largely missing from the basal region of cochlear OHCs where high frequencies are encoded
• however, ESPN is present at P9 stereocilia tips at similar levels in apical and basal hair bundles
• at P10.5 and P30.5, basal cochlear OHC bundles only have two rows of stereocilia, except for scattered row 3 stereocilia
• however, all inner hair cells (IHCs) and OHCs from mid regions and the apex appear normal
• at P30, mice show significantly increased ABR thresholds at 32 kHz relative to wild-type controls
• at P30, mice show high-frequency hearing loss

nervous system
• at P10.5 and P30.5, the shortest row (row 3) of stereocilia is largely missing from the basal region of cochlear OHCs where high frequencies are encoded
• however, ESPN is present at P9 stereocilia tips at similar levels in apical and basal hair bundles
• at P10.5 and P30.5, basal cochlear OHC bundles only have two rows of stereocilia, except for scattered row 3 stereocilia
• however, all inner hair cells (IHCs) and OHCs from mid regions and the apex appear normal




Genotype
MGI:7610482
ht2
Allelic
Composition
Espnlem1Pgg/Espnlem2Pgg
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Espnlem1Pgg mutation (1 available); any Espnl mutation (30 available)
Espnlem2Pgg mutation (0 available); any Espnl mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• at P30, mice show significantly increased ABR thresholds at 32 kHz relative to wild-type controls
• at P30, mice show high-frequency hearing loss





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory