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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Qkiqk-v
quaking viable
MGI:1856539
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Qkiqk-v/Qkiqk-v B6C3Fe a/a-Qkiqk-v/J MGI:3698852
hm2
Qkiqk-v/Qkiqk-v involves: C3H/Di * DBA/2J MGI:3758073
hm3
Qkiqk-v/Qkiqk-v involves: DBA/2 MGI:6459893
hm4
Qkiqk-v/Qkiqk-v involves: DBA/2J MGI:2674329
cx5
Qkiqk-v/Qkiqk-v
Tg(PGK2-Pacrg)#Jus/?
involves: BTBR * C57BL/6J * DBA/2 MGI:5286587
cx6
Del(17)TOrl/+
Qkiqk-v/Qki+
involves: C57BL/6J * Orl:Swiss MGI:3798959


Genotype
MGI:3698852
hm1
Allelic
Composition
Qkiqk-v/Qkiqk-v
Genetic
Background
B6C3Fe a/a-Qkiqk-v/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Qkiqk-v mutation (2 available); any Qki mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Brain morphology in Qkie5/Qkie5 and Qkiqk-v/Qkiqk-v mice

hearing/vestibular/ear
• prolonged latency for all peaks and larger amplitudes for P1/N1

nervous system
• onset of seizures begins at 6-8 weeks of age; seizures occur less frequently than in homozygous Qke5 mice
• aging mutants exhibit Purkinje cell axonal swellings, indicating neurodegeneration
• decrease in myelination, however more axons are surrounded by thin myelin sheaths than seen in Qke5 homozygotes (J:102038)
• microsomes prepared from brains of 18 day old homozygotes show a reduction in fatty acid chain elongation activity with arachidoyl CoA, behenoyl CoA, and palmitoyl CoA substrates (J:160743)

behavior/neurological
• onset of seizures begins at 6-8 weeks of age; seizures occur less frequently than in homozygous Qke5 mice

reproductive system
• the testis contain many spermatogenic cells, but few spermatozoa and the spermatozoa collected from the cauda epididymis all have abnormal heads and/or tails and less than 0.5% are barely motile, and although in vitro fertilization is not successful, intracytoplasmic sperm injection and round spermatid injection are successful in production of offspring from homozygous males

cellular




Genotype
MGI:3758073
hm2
Allelic
Composition
Qkiqk-v/Qkiqk-v
Genetic
Background
involves: C3H/Di * DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Qkiqk-v mutation (2 available); any Qki mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• following swimming, some mice become motionless and then display a tonic extension of hindlimbs for several minutes
• some mice exhibit adduction of limbs under a flexed trunk and then become stiff and motionless for several seconds
• region from olfactory bulb to sacral spinal cord is deficient in myelin at all ages studied (12 days to 4 months)
• loss of myelination begins at the junction of peripheral and central nervous systems
• cranial and spinal nerves (except optic nerve) are myelinated
• some fragments of myelin are seen in almost all fiber tracts
• cells in white matter and grey matter tracts appear normal

behavior/neurological
• tremors are most evident in the caudal part of the trunk and proximal portions of hind extremities
• visually, the rate of tremors are 2 to 3 per second
• tremors are first observed at 10-12 days of age and reach full expression by 3 weeks
• in some animals, tremors diminish at 3 months
• physical contact with the mouse reduces or stops tremors
• some animals exhibit hindlimb weakness at 3 months of age
• following swimming, some mice become motionless and then display a tonic extension of hindlimbs for several minutes
• some mice exhibit adduction of limbs under a flexed trunk and then become stiff and motionless for several seconds

reproductive system
• male homozygotes rarely sire offspring




Genotype
MGI:6459893
hm3
Allelic
Composition
Qkiqk-v/Qkiqk-v
Genetic
Background
involves: DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Qkiqk-v mutation (2 available); any Qki mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system




Genotype
MGI:2674329
hm4
Allelic
Composition
Qkiqk-v/Qkiqk-v
Genetic
Background
involves: DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Qkiqk-v mutation (2 available); any Qki mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• decrease in the frequency of exploratory sniffing (at wire mesh or a novel object) and leans against the novel object in males
• increase in the frequency of hair fluffing in males
• decrease in the frequency of leaning against the wall or a novel object and single forepaw lifts in males
• decrease in the frequency of wire mesh climbing in males
• walk slowly with a trembling gait




Genotype
MGI:5286587
cx5
Allelic
Composition
Qkiqk-v/Qkiqk-v
Tg(PGK2-Pacrg)#Jus/?
Genetic
Background
involves: BTBR * C57BL/6J * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Qkiqk-v mutation (2 available); any Qki mutation (26 available)
Tg(PGK2-Pacrg)#Jus mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
N
• all males are fertile and sire a normal number of litters
• average litter size is similar to wild type controls
• sperm titers are reduced about 30% relative to wild type controls but are considerably higher than in the absence of the transgene

cellular
• sperm titers are reduced about 30% relative to wild type controls but are considerably higher than in the absence of the transgene




Genotype
MGI:3798959
cx6
Allelic
Composition
Del(17)TOrl/+
Qkiqk-v/Qki+
Genetic
Background
involves: C57BL/6J * Orl:Swiss
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Del(17)TOrl mutation (1 available); any Del(17)TOrl mutation (1 available)
Qkiqk-v mutation (2 available); any Qki mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice heterozygous for T and Qk display tremors characteristic of the recessive mutation QK, demonstrating that T comprises a deletion

limbs/digits/tail





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory