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Phenotypes Associated with This Genotype
Genotype
MGI:3611474
Allelic
Composition
Kcnq1vtg-3J/Kcnq1vtg-3J
Genetic
Background
C57BL/6J-Kcnq1vtg-3J/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kcnq1vtg-3J mutation (1 available); any Kcnq1 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• from approximately 3.7 weeks of age, mutant mice exhibit a noticeable body tremor
• mutant mice sometimes lean slightly to the side
• homozygous mice occasionally lift both hind limbs simultaneously
• homozygous mutant mice occasionally exhibit backward locomotion

hearing/vestibular/ear
• examination of sections of the ears reveals severe malformation of the cochlea, with collapse of the cochlear ducts
• examination of sections of the ears reveals severe malformation of the vestibular region, with collapse of the the endolymphatic portion of the vestibular system
• examination of the whole ear revealed abnormal otoconia


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
12/17/2024
MGI 6.24
The Jackson Laboratory