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Phenotypes Associated with This Genotype
Genotype
MGI:6113291
Allelic
Composition
Slc25a13hspn/Slc25a13hspn
Genetic
Background
B6.SJL(C)-Slc25a13hspn/Kjn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Slc25a13hspn mutation (1 available); any Slc25a13 mutation (179 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• fail to orient in water
• rapid circling

nervous system
• at 4 weeks of age there are only occassional missing hair bundles throughout the basal and middle turns of the cochlea, but there is an additional 4th or sometimes 5th row of outer hair cells in the apical turn where there can also be abnomral orientation of hair bundles

hearing/vestibular/ear
• at 5 weeks of age the inner ears are small and malformed, the cochlea has fewer turns than normal and appears swollen, all 3 semicircular canals are either absent, smaller, or malformed
• at 4 weeks of age there are only occassional missing hair bundles throughout the basal and middle turns of the cochlea, but there is an additional 4th or sometimes 5th row of outer hair cells in the apical turn where there can also be abnomral orientation of hair bundles
• all 3 semicircular canals are either absent, reduced or malformed
• absent in 6 of 7 embryos assessed at E15.5
• absent in 6 of 7 embryos at E15.5
• embryonic day 15.5 absent in all of 7 embryos
• embryonic day 15.5 absent in all of 7 embryos
• at 4 to 5 weeks of age no ABR wave patterns detectable for pure tone 8, 16, or 32 kHz even at 100 dB


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)
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last database update
01/28/2026
MGI 6.24
The Jackson Laboratory