Phenotypes Associated with This Genotype

Genotype
MGI:6102907

• Allelic Composition: Emx2^Pdo/Emx2⁺
• Genetic Background: involves: BALB/c

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

hearing/vestibular/ear

abnormal middle ear ossicle morphology ( J:250208 )

abnormal incus morphology ( J:250208 )

abnormal malleus morphology ( J:250208 )

abnormal stapes morphology ( J:250208 )

abnormal cochlea morphology ( J:250208 )

increased cochlear outer hair cell number ( J:250208 )

• in the apical and middle turns of the cochlea

abnormal cochlear inner hair cell morphology ( J:250208 )

• some appearing to form a second row

increased cochlear nerve compound action potential ( J:250208 )

impaired hearing ( J:250208 )

nervous system

increased cochlear outer hair cell number ( J:250208 )

• in the apical and middle turns of the cochlea

abnormal cochlear inner hair cell morphology ( J:250208 )

• some appearing to form a second row

increased cochlear nerve compound action potential ( J:250208 )

craniofacial

abnormal middle ear ossicle morphology ( J:250208 )

abnormal incus morphology ( J:250208 )

abnormal malleus morphology ( J:250208 )

abnormal stapes morphology ( J:250208 )

skeleton

abnormal middle ear ossicle morphology ( J:250208 )

abnormal incus morphology ( J:250208 )

abnormal malleus morphology ( J:250208 )

abnormal stapes morphology ( J:250208 )