Strain Name:

C3H/HeJ-snol/J

Stock Number:

004476

Availability:

Repository- Live

Description

Strain Information

Former Names C3H/HeJ-snol    (Changed: 15-DEC-04 )
C3H/HeJ-snol/snol    (Changed: 15-DEC-04 )
Type Coisogenic; Mutant Strain; Spontaneous Mutation;
Additional information on Genetically Engineered Mutant Mice.
Specieslaboratory mouse
H2 Haplotypek
GenerationF8+N6F1 (07-DEC-07)

Appearance
agouti, snubnosed with malocclusion
Related Genotype: A/A snol/snol

agouti, unaffected
Related Genotype: A/A snol/+ or A/A +/?

Important Note
The C3H/HeJ background strain is homozygous for the retinal degeneration 1 mutation, Pde6brd1.

Description
The snol homozygous mutant phenotype includes a short nose, odd face and body shape, and kinked tail. Most mutants also get malocclusion and two homozygous mutants tested at 49 days of age exhibited intermediate hearing loss ( about 25 dB above normal). The odd shape of the face can be used to distinguish the Homozygotes by 14 days of age. snol has been mapped to Chromosome 4. The most likely gene order places the mutation between D4Mit12 and D4Mit203 in 92 tested meioses. A short nosed mutation, snubnose (sno), maps in this location, but could not be tested for allelism because it is believed to be extinct. The spina bifida occulta reported in sno homozygotes is not seen in snol homozygotes.

Control Information

  Control
   Heterozygote from the colony
   Untyped from the colony
   000659 C3H/HeJ
 
  Considerations for Choosing Controls

Phenotype

Phenotype Information

View Mammalian Phenotype Terms

Mammalian Phenotype Terms
      assigned by genotype

snol/snol

        C3H/HeJ
  • lethality-postnatal
  • postnatal lethality (MGI Ref ID J:78986)
    • incomplete penetrance; some mutant mice die by weaning age, although others may survive to adulthood and breed
  • craniofacial phenotype
  • abnormal head morphology (MGI Ref ID J:78986)
    • homozygous mutants are recognizable at about 14 days of postnatal development by their odd shaped face
    • short snout (MGI Ref ID J:78986)
      • mice are described as having a short snout
  • malocclusion (MGI Ref ID J:78986)
    • most mutant mice get malocclusion
  • growth/size phenotype
  • abnormal postnatal growth/weight/body size (MGI Ref ID J:78986)
    • mice are described as having an odd body shape
  • hearing/vestibular/ear phenotype
  • decreased brainstem auditory evoked potential (MGI Ref ID J:78986)
    • ABR results showed that two homozygous mutant mice tested at 49 days of age exhibited intermediate hearing loss (about 25 dB above normal) and two +/? littermate control mice had normal hearing
  • limbs/digits/tail phenotype
  • kinked tail (MGI Ref ID J:78986)
  • skeleton phenotype
  • malocclusion (MGI Ref ID J:78986)
    • most mutant mice get malocclusion
View Research Applications

Research Applications
This mouse can be used to support research in many areas including:

snol related

Developmental Biology Research
Craniofacial and Palate Defects
Skeletal Defects

Genes & Alleles

Gene & Allele Information

Allele Symbol snol
Allele Name snubnose-like
Allele Type Spontaneous
Strain of OriginC3H/HeJ
General Note

A short nosed mutation, snubnose (sno), maps in this location, but could not be allele tested because it is believed to be extinct. The spina bifida occulta reported in sno is not seen in snol.

Molecular Note A spontaneous mutation discovered at The Jackson Laboratory.

Genotyping

Genotyping Information

This strain will not have a genotyping protocol or one is not currently available.

Helpful Links

Optimizing PCR Protocols

References

References

Selected Reference(s)

Ward-Bailey PF; Harris B; Donahue LR; Bronson R; Curtain M; Johnson K; Davisson M. 2002. Snubnose-like (snol): a new spontaneous skeletal mutation on Chromosome 4 in the mouse. Mouse Mutant Resources Web Site, The Jackson Laboratory, Bar Harbor, Maine (http://www.jax.org/mmr) MGI Direct Data Submission :.  [MGI Ref ID J:78986]

Health & husbandry

Health & Colony Maintenance Information

Animal Health Reports

Room Number           A1

Purchasing information

Pricing, Supply Level & Notes, Controls, General Terms & Conditions

Pricing

Pricing for USA, Canada and Mexico shipping destinations View International pricing
Weeks of AgePrice*GenderGenotypes Provided
Individual Mouse Price $199.30Female or MaleHomozygous for snol
Pairs /Price*Pair Genotype
$218.70C3H/HeJ (000659) x Homozygous for snol
$216.85Homozygous for snol x C3H/HeJ (000659)
$251.60Heterozygous for snol x Heterozygous for snol
*Price(s) in US dollars ($)

Additional Supply Details

Supply Notes

Pricing for International shipping destinations View USA Canada and Mexico pricing
Weeks of AgePrice*GenderGenotypes Provided
Individual Mouse Price $259.10Female or MaleHomozygous for snol
Pairs /Price*Pair Genotype
$284.40C3H/HeJ (000659) x Homozygous for snol
$282.00Homozygous for snol x C3H/HeJ (000659)
$327.10Heterozygous for snol x Heterozygous for snol
*Price(s) in US dollars ($)

Additional Supply Details

Supply Notes

Supply Details

Standard SupplyRepository-Live. A collection of over 1000 strains maintained as live colonies. Individual colonies are sized to meet current customer demand. Delivery for orders of 10 mice or less ranges on average from one to eight weeks; mice are generally shipped between four to six weeks of age with a maximum shipping age of ~nine weeks. Colony sizes do not generally support stringent age specifications for large volumes of mice; however custom orders and larger quantities of mice are easily arranged. Estimated ship dates for all orders provided within 48 hours of order placement.
Supply Notes
Important NoteThe C3H/HeJ background strain is homozygous for the retinal degeneration 1 mutation, Pde6brd1.

Control Information

  Control
   Heterozygote from the colony
   Untyped from the colony
   000659 C3H/HeJ
 
  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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