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Phenotypes Associated with This Genotype
Genotype
MGI:3033376
Allelic
Composition
Slc12a7tm1Tjj/Slc12a7tm1Tjj
Genetic
Background
involves: 129/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Slc12a7tm1Tjj mutation (0 available); any Slc12a7 mutation (67 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• normal vestibular and motor function
• absent Pinna reflex in adult mice

growth/size/body
• approximately 90% that of wild-type littermates

hearing/vestibular/ear
• Reissner's membrane remained intact
• near absence of the outer hair cells of the basal turns of the cochlea by 21 days of age
• inner hair cells were still present at the basal turns of the cochlea at 21 days of age
• degeneration proceeded from basal to apical turns of cochlea
• some inner hair cells persisted in the cochlear apical turns in adult mice, and most likely account for the observed residual hearing
• completely absent in basal turns
• ABR responses are normal at P14, but deteriorate rapidly thereafter, with a hearing loss of 70-80 dB
• while hearing was normal at 14 days of age, it deteriorated during the third week of life
• mice were nearly deaf by 21 days of age

homeostasis/metabolism
• putatively due to impaired chloride recycling across the basolateral membrane of acid secreting alpha-intercalated cells of the distal nephron
• increased alkalinity
• normal levels of Na+, K+, Cl-

renal/urinary system
• putatively due to impaired chloride recycling across the basolateral membrane of acid secreting alpha-intercalated cells of the distal nephron
• increased alkalinity
• normal levels of Na+, K+, Cl-

vision/eye
N
• normal vision

nervous system
• near absence of the outer hair cells of the basal turns of the cochlea by 21 days of age
• inner hair cells were still present at the basal turns of the cochlea at 21 days of age
• degeneration proceeded from basal to apical turns of cochlea
• some inner hair cells persisted in the cochlear apical turns in adult mice, and most likely account for the observed residual hearing
• degeneration of the neurons of the cochlear ganglion


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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
04/23/2024
MGI 6.23
The Jackson Laboratory