Strain Name:

129S8/SvEv-Gpi1c Hprt1b-m2/J

Stock Number:

002027

Availability:

Repository-Cryopreserved

Description

Strain Information

Former Names 129S8/SvEv-Gpi1c Hprtb-m2/J    (Changed: 23-NOV-05 )
129S8/SvEv@J-Gpi1c Hprtb-m2    (Changed: 15-DEC-04 )
Type Insertion;
Additional information on Mice with Chromosomal Aberrations.
Type Mutant Strain;
Additional information on Genetically Engineered Mutant Mice.
Specieslaboratory mouse
Generation?+F5p

Development
The Hprt1b-m2 mutation was induced in ES cells by retroviral insertion.

Control Information

  Control
   002448 129S1/SvImJ (approximate)
 
  Considerations for Choosing Controls

Related Strains

View Strains carrying other alleles of Gpi1     (14 strains)

Strains carrying other alleles of Hprt1
004302   129S1-Hprt1tm1(cre)Mnn/J
002171   B6.129P2-Hprt1b-m3/J
003138   B6;129-Hprt1tm1Detl/J
000807   RBJ/DnJ
View Strains carrying other alleles of Hprt1     (4 strains)

Additional Web Information

New 129 Nomenclature Bulletin

Phenotype

Phenotype Information

View Mammalian Phenotype Terms

Mammalian Phenotype Terms
      assigned by genotype

The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.

Hprt1b-m2/Y

        involves: 129S/SvEv
  • behavior/neurological phenotype
  • *normal* behavior/neurological phenotype (MGI Ref ID J:15485)
    • mice exhibit normal behavior

Hprt1b-m2/Y

        involves: 129 * 129S/SvEv
  • nervous system phenotype
  • decreased dopamine level (MGI Ref ID J:115724)
    • striatal concentrations of dopamine are lower than in wild-type mice
  • behavior/neurological phenotype
  • *normal* behavior/neurological phenotype (MGI Ref ID J:115724)
    • mice exhibit overall similar behavior as observed in wild-type mice in open field, bridge, passive avoidance and apomorphine-induced activity tests
    • abnormal locomotor activation (MGI Ref ID J:115724)
      • male mice spend less time in the center of an open field than Hprt1b-m1 male mice
    • abnormal motor coordination/ balance (MGI Ref ID J:115724)
      • male mice make more slips when climbing than escape platform in a swim test compared to Hprt1b-m1 male mice
View Research Applications

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

Mouse/Human Gene Homologs
Lesch-Nyhan syndrome

Genes & Alleles

Gene & Allele Information

Allele Symbol Gpi1c
Allele Name c variant
Allele Type Not Applicable
Strain of Originwild
Gene Symbol and Name Gpi1, glucose phosphate isomerase 1
Chromosome 7
Gene Common Name(s) AMF; GNPI; Gpi-1; Gpi-1r; Gpi-1s; Gpi-1t; Gpi1-r; Gpi1-s; Gpi1-t; MF; NK; NK/GPI; NLK; Org; PGI; PHI; SA-36; autocrine motility factor; glucose phosphate isomerase 1, regulatory; glucose phosphate isomerase 1, structural; glucose phosphate isomerase 1, temporal; maturation factor; neuroleukin;
Molecular Note This allele determines a fast migrating variant of the encoded enzyme and occurs in the wild.
 
Allele Symbol Hprt1b-m2
Allele Name hypoxanthine guanine phosphoribosyl transferase B, mutation 2
Allele Type Transgenic (random, gene disruption)
Common Name(s) Hprt-bm2; hprtmb2;
Strain of Origin129S/SvEv-Gpi1
ES Cell Line NameCCE/EK.CCE
ES Cell Line Strain129S/SvEv-Gpi1
Gene Symbol and Name Hprt1, hypoxanthine guanine phosphoribosyl transferase 1
Chromosome X
Gene Common Name(s) C81579; HGPRT; HPGRT; HPRT; Hgprtase; MGC112554; expressed sequence C81579;
Molecular Note A retroviral sequence was inserted into intron 5. [MGI Ref ID J:3354]

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)

Williamson DJ; Hooper ML; Melton DW. 1992. Mouse models of hypoxanthine phosphoribosyltransferase deficiency. J Inherit Metab Dis 15(4):665-73. [PubMed: 1528024]  [MGI Ref ID J:3354]

Additional References

Gpi1c related

Padua RA; Bulfield G; Peters J. 1978. Biochemical genetics of a new glucosephosphate isomerase allele (Gpi-1c) from wild mice. Biochem Genet 16(1-2):127-43. [PubMed: 25645]  [MGI Ref ID J:5973]

Hprt1b-m2 related

Finger S; Heavens RP; Sirinathsinghji DJ; Kuehn MR; Dunnett SB. 1988. Behavioral and neurochemical evaluation of a transgenic mouse model of Lesch-Nyhan syndrome. J Neurol Sci 86(2-3):203-13. [PubMed: 3221240]  [MGI Ref ID J:115724]

Kuehn MR; Bradley A; Robertson EJ; Evans MJ. 1987. A potential animal model for Lesch-Nyhan syndrome through introduction of HPRT mutations into mice. Nature 326(6110):295-8. [PubMed: 3029599]  [MGI Ref ID J:15485]

Zheng B; Mills AA; Bradley A. 1999. A system for rapid generation of coat color-tagged knockouts and defined chromosomal rearrangements in mice. Nucleic Acids Res 27(11):2354-60. [PubMed: 10325425]  [MGI Ref ID J:115976]

Health & husbandry

Health & Colony Maintenance Information

Currently there no information available for this strain. This may be due to the supply level of this strain.

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*Gender
Cryorecovery Fee $1900.00
*Price(s) in US dollars ($)

Additional Supply Details

Pricing for International shipping destinations View USA Canada and Mexico pricing
Weeks of AgePrice*Gender
Cryorecovery Fee $2470.00
*Price(s) in US dollars ($)

Additional Supply Details

Supply Details

Standard SupplyRepository-Cryopreserved. Must Be Recovered. Please refer to pricing and supply notes for further information.
Supply Notes
  • Cryorecovery - Standard.
    The recovery process begins when a signed agreement form is returned to the Customer Service Department after order placement. Although results vary by strain, at least two males and two females (two pairs) will be provided, typically within 15 weeks of our receipt of the signed agreement form. If the first recovery attempt is unsuccessful or only one pair is recovered, a second recovery will be done, extending the delivery time to approximately 25 weeks. At least one member of each pair will be of known genotype and will carry the mutation if it is a mutant strain. Please note that pairs may not reflect the mating scheme utilized by The Jackson Laboratory prior to cryopreservation of the strain. Mating schemes are sometimes modified for successful cryopreservation. Price represents a repository maintenance fee, which includes the cost of recovery of the strain from the cryopreservation resource and the periodic replacement of the frozen embryos used for recovery.

    Cryorecovery to establish a Dedicated Supply for greater quantities of mice.
    One to two pairs will be recovered to establish a Dedicated Supply of mice. Price by quotation. For more information on Dedicated Supply, please contact JAX® Services, Tel: 1-800-422-6423 or 1-207-288-5845.

  • Genomic DNA is available for this strain from the Mouse DNA Resource.

Control Information

  Control
   002448 129S1/SvImJ (approximate)
 
  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.

General Terms and Conditions


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The Jackson Laboratory has rigorous genetic quality control and mutant gene genotyping programs to ensure the genetic background of JAX® Mice strains as well as the genotypes of strains with identified molecular mutations. JAX® Mice strains are only made available to researchers after meeting our standards. However, the phenotype of each strain may not be fully characterized and/or captured in the strain data sheets. Therefore, we cannot guarantee a strain's phenotype will meet all expectations. To ensure that JAX® Mice will meet the needs of individual research projects or when requesting a strain that is new to your research, we suggest ordering and performing tests on a small number of mice to determine suitability for your particular project.
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Contact Information
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Fax: 207.288.6150
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Terms of Use

Terms of Use


General Terms and Conditions


Contact information

General inquiries

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phone:207-288-6470
fax:207-288-6655

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