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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Sptbn5tm1.1Dsna
targeted mutation 1.1, Dhasakumar S Navaratnam
MGI:7596140
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Sptbn5tm1.1Dsna/Sptbn5tm1.1Dsna involves: 129S/SvEv * C57BL/6J MGI:7596141


Genotype
MGI:7596141
hm1
Allelic
Composition
Sptbn5tm1.1Dsna/Sptbn5tm1.1Dsna
Genetic
Background
involves: 129S/SvEv * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sptbn5tm1.1Dsna mutation (0 available); any Sptbn5 mutation (59 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• ABR wave I amplitudes from 5.6 kHz and upwards are reduced at high stimulus intensities (suprathreshold)
• however, ABR thresholds are unaltered across all sound frequencies tested, distortion product otoacoustic emissions (DPOAEs), even at sound intensities of 80-90 dB SPL, are unaffected in 2-month-old mice and, adolescent and adult mice exhibit normal nonlinear capacitance characteristics indicating a neuronal processing issue and not outer hair cell dysfunction

nervous system
• mice show a reduction in neurofilament labeled, nonmyelinated, afferent nerve fibers at the habenular in all three turns of the cochlea, as well as efferent nerve fibers, in the basal and middle turns of the cochlea
• however, no difference in the number of inner hair cell ribbon synapses in the basal, middle, and apical turn of the organ of Corti are seen





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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
05/07/2024
MGI 6.23
The Jackson Laboratory