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Type Coisogenic; Mutant Strain; Spontaneous Mutation; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Species laboratory mouse Generation N17F4N1p (29-FEB-04) Appearance
agouti
Related Genotype: A/ADescription
Mice homozygous for the vestibulomotor degeneration spontaneous mutation (wlvmd) can be identified at 20 days of age by their small size, shaky behavior, ungroomed coat, and emaciation. Homozygous mutant mice tend to sit hunched with rear feet and limbs tucked in towards the body and exhibit a generalized tremor. When startled, they jump sideways. They clasp their hind feet when picked up by the tail. Most mutants die by 30 days of age, probably from inability to feed and starvation. There is no apparent difference between the wabbler lethal (wl) and vestibulomotor degeneration mutant phenotypes.
| Control | ||
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| Untyped from the colony | ||
| Considerations for Choosing Controls | ||
Strains carrying other alleles of wl
004835 B6 x B6JCu.Cg-wl/J 002457 CBA/J-wl3J/J 000147 WLHR/LeJ View Strains carrying other alleles of wl (3 strains)
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
wlvmd/wlvmd
C3H/HeSnJ-wlvmd/J
- life span-post-weaning/aging
- premature death (MGI Ref ID J:11718)
- few survive longer than 30 days of age, presumably due to starvation as homozygotes are unable to feed themselves
- growth/size phenotype
- decreased body size (MGI Ref ID J:11718)
- smaller size is identifiable at 20 days of age
- cachexia (MGI Ref ID J:11718)
- seen by 20 days of age
- nervous system phenotype
- axonal dystrophy (MGI Ref ID J:11718)
- dystrophic axons are concentrated in the ventral funiculus of the cervical segments of the spinal cord and are particularly numerous in ventro-medial aspects of the medulla dorsal to the pyramids and ventral to the medial lemniscus in the area of the vestibulospinal tract
- axons in the vestibular spinal tract and some axons projecting from the vestibular ganglion to the lateral vestibular nucleus are dystrophic
- chromatolysis (MGI Ref ID J:11718)
- neurons in both the vestibular ganglion and nucleus have central chromatolysis
- motor neuron degeneration (MGI Ref ID J:11718)
- vestibulo-motor degeneration
- behavior/neurological phenotype
- abnormal involuntary movement (MGI Ref ID J:11718)
- when startled, jump sideways with legs splay out from the body
- limb grasping (MGI Ref ID J:11718)
- when picked up by tail, clasp hind legs and the entire body shakes violently
- tremors (MGI Ref ID J:11718)
- exhibit a generalized tremor
- decreased eating behavior (MGI Ref ID J:11718)
- unable to feed themselves leading to starvation
- hunched posture (MGI Ref ID J:11718)
- tend to sit hunched over with rear feet and legs tucked in towards the body
- skin/coat/nails phenotype
- disheveled coat (MGI Ref ID J:11718)
- ungroomed hair coat
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:wlvmd related
Neurobiology Research
Ataxia (Movement) Defects
Myelination Defects
Neurodegeneration
Tremor Defects
| Allele Symbol | wlvmd | ||
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| Allele Name | vestibulomotor degeneration | ||
| Allele Type | Spontaneous | ||
| Common Name(s) | vmd; | ||
| Strain of Origin | C3H/HeSnJ | ||
| Gene Symbol and Name | wl, wabbler-lethal | ||
| Chromosome | 14 | ||
| Gene Common Name(s) | vestibulomotor degeneration; vmd; | ||
| General Note | This allele of wl arose in the C3H/HeSnJ strain at The Jackson Laboratory.(J:11718). No lesions have been found in somatic organs (J:2856). There is no apparent difference between the wl/wl and wlvmd/wlvmd phenotypes (J:28233). | ||
This strain will not have a genotyping protocol or one is not currently available.
Helpful Links
Optimizing PCR Protocols
Bronson RT; Sweet HO; Spencer CA; Davisson MT. 1992. Genetic and age related models of neurodegeneration in mice: dystrophic axons. J Neurogenet 8(2):71-83. [PubMed: 1634998] [MGI Ref ID J:11718]
wlvmd relatedBronson RT; Sweet HO; Spencer CA; Davisson MT. 1992. Genetic and age related models of neurodegeneration in mice: dystrophic axons. J Neurogenet 8(2):71-83. [PubMed: 1634998] [MGI Ref ID J:11718]
Carroll EW; Curtis RL; Sullivan DA; Melvin JL. 1992. Wallerian degeneration in the optic nerve of the wabbler-lethal (wl/wl) mouse. Brain Res Bull 29(3-4):411-8. [PubMed: 1382814] [MGI Ref ID J:2856]
Sweet HO. 1993. Vestibulo-motor degeneration Mouse Genome 91(4):860. [MGI Ref ID J:28233]
Currently there no information available for this strain. This may be due to the supply level of this strain.
| Pricing for USA, Canada and Mexico shipping destinations |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $1900.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
| Pricing for International shipping destinations |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $2470.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
| Standard Supply | Cryopreserved. Ready for recovery. Please refer to pricing and supply notes for further information. |
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| Supply Notes |
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| Control | ||
|---|---|---|
| Untyped from the colony | ||
| Considerations for Choosing Controls | ||
| USA, Canada and Mexico - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
| International - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
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Technical Support Email Form
| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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