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Strain Name:

B6.A-H2-T18a.HRS-Hrhr/J

Stock Number:

001737

Availability:

Repository-Cryopreserved


General Terms and Conditions

Former Name      B6.A-H2-T18a.HRS-Hr/J    (Changed: 15-DEC-04 )
      B6.A-H2-T18a.HRS-hr/J    (Changed: 15-DEC-04 )
Genes & Alleles   H2-T18;   Hr;   Hrhr;   ;


Product Information

Strain Details

Type JAX® GEMM® Strain - Congenic
Additional information on JAX® GEMM® Strains.
Type JAX® GEMM® Strain - Major Histocompatibility Congenic
Type JAX® GEMM® Strain - Mutant Strain
Type JAX® GEMM® Strain - Spontaneous Mutation
Specieslaboratory mouse
Background Strain C57BL/6
Donor Strain T18a, A; Hrhr, HRS
GenerationN15 F3p

Strain Description
Mice homozygous for the hr mutation have a higher incidence and earlier onset of leukemia, reducible by virus-specific antibody. Deficiency of splenic T helper cells (Ly-1+) may account for low cellular immune response of homozygous mutant mice. The coat is normal on hr/hr mice up to 10 days but then hair is lost from the follicle. Waves of hair growth with few thin fuzzy hairs ocur at monthly intervals for some time but homozygotes eventually become continuously hairless. Vibrissae are repeatedly regrown and shed, becoming more abnormal with age. Toenails are long and curved. There is hyperkeratosis of statified epithelium and the upper part of hair canals beginning at 14 days. Hair club formation is abnormal. Cysts form from the hyperkeratotic upper part of hair canals and sheaths of abnormal follicles stranded in dermis. Some cysts also form from sebaceous glands. All cysts undergo sebaceous transformation and later keratinization. In an attempt to offer alleles on well-characterized or multiple genetic backgrounds, alleles are frequently moved to a genetic background different from that on which an allele was first characterized. This is the case for the strain above. It should be noted that the phenotype could vary from that originally described. We will modify the strain description if necessary as published results become available.

Related Disease (OMIM) Terms

Alopecia Universalis Congenita; ALUNC
Atrichia with Papular Lesions; APL
Mammalian Phenotype Terms assigned by genotype

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

Hrhr/Hrhr

        Background Not Specified
  • behavior/neurological phenotype
  • abnormal nursing (J:2409)
    • failure
  • endocrine/exocrine gland phenotype
  • abnormal mammary gland morphology (J:2409)
    • small
    • nipple at bottom of cup-shaped depression in skin
    • no ducts
  • sebaceous gland atrophy (J:2409)
  • reproductive system phenotype
  • abnormal mammary gland morphology (J:2409)
    • small
    • nipple at bottom of cup-shaped depression in skin
    • no ducts
  • skin/coat/nails phenotype
  • abnormal skin morphology (J:2409)
    • thickened cutis
    • abnormal stratum reticulare morphology (J:2409)
      • cystic
    • dermal cysts (J:14889)
    • epidermal hyperplasia (J:14940)
    • hyperkeratosis (J:14940)
    • sebaceous gland atrophy (J:2409)
  • alopecia (J:2409)
    • beginning ~15 days of age and progressing from nose back
  • deformed nails (J:2409)
    • curved

Hrhr/Hrhr

        HRS/J Hrhr
  • tumorigenesis
  • leukemia (J:5726)
    • increased incidence
    • increased incidence
  • immune system phenotype
  • decreased T cell number (J:6087)
    • of CD5+ T cells
  • decreased T cell proliferation (J:6375)
    • to alloantigens by T helper cells
  • hematopoietic system phenotype
  • decreased T cell number (J:6087)
    • of CD5+ T cells
  • decreased T cell proliferation (J:6375)
    • to alloantigens by T helper cells

Hrhr/Hrhr

        HRS/J
  • hearing/vestibular/ear phenotype
  • absent linear vestibular evoked potential (J:116914)
    • VESPs are absent at the maximum stimulus intensity used

Gene & Allele Details

Allele Symbol Hrhr
Allele Name hairless
Common Name(s) hr;
Gene Symbol and Name Hr, hairless
Chromosome 14
Gene Common Name(s) ALUNC; AU; HSA277165; N; ba; baldy; bldy; rh; rh-bmh; rhino-bald Mill Hill;
General Note Homozygous Hrhr/Hrhr mice develop a normal coat up to the age of about 10 days, but then lose all hair. The complete hair is lost from the follicle, not merely broken off. Waves of hair growth producing a few thin fuzzy hairs occur at intervals of about a month for some time thereafter, but the animals eventually appear continuously hairless (J:2409).The vibrissae are repeatedly regrown and shed, and become more abnormal with age. Toenails are excessively long and curved. There ishyperkeratosis of the stratified epithelium and upper part of the hair canals beginning at about 14 days. Hair club formation is abnormal, with the internal root sheath coalescing around the terminal part of the hair shaft so that the lower part of the external root sheath fails to follow the ascending hair club and becomes stranded in the dermis. Cysts develop from two sources, the hyperkeratotic upper part of the hair canals, and the sheaths of the abnormal follicles stranded in the dermis (J:14940, J:5239). Some cysts arise from isolated sebaceous glands. Regardless of their origin, all cysts undergo a sebaceous transformation and later a keratinization (J:14889).Hairless mice are generally fertile, but most females do not nurse their young well (J:2409).Homozygous hairless mice of the inbred HRS/J strain have a higher incidence of leukemia with earlier onset than their normal sibs, a 13-fold higher titer of ecotropic virus in tail extracts at 6 months of age (J:5726), a 100-fold higher titer of xenotropic virus in the thymus at 8 months of age (J:5908), and a lower cellular immune response to tumor viruses that may be responsible for the increased tumor susceptibility of the mice (J:6535). The incidence of leukemia in Hr homozygotes can be significantly reduced by passive immunization with virus-specific antiserum (J:6059). The lower cellular immune response of these mice is characteristic of spleen cells but not of lymph node cells and is due to a deficiency of T helper (Ly-1+) cells (J:6375, J:6087).The Hrhr mutation was caused by a retroviral integration, as shown by the complete concordance of the mutation and the provirus in several strains carrying Hr and the excision of the provirus in a haired revertant (J:9252). The gene mutated in hr has been identified and cloned. Its predicted protein product has 1182 amino acids, and includes a zinc finger domain. Expression sites are consonant with the sites of abnormalities in hairless mutants (J:19624). The Hrhr mutation disrupts the integrity of tissues in the hair follicle (J:47743).
Molecular Note Mice homozygous for hr contain one or more MLV proviruses closely linked to this allele. Molecular analysis of an hr (haired) revertant showed the presence of only a single proviral, MX40, LTR establishing a causal relationship between the viral integration and the hr mutant allele. [J:92053] [J:9252]
Gene Symbol and Name H2-T18, histocompatibility 2, T region locus 18
Chromosome 17
Gene Common Name(s) H-2T18; TL Ag; Tla; thymus leukemia antigen;

Control Information

  Allele   Control
 Hrhr  000664 C57BL/6J
   000664 C57BL/6J
 
  Considerations for Choosing Controls

Related Strains

Strains carrying   Hrhr allele
002922   D2.HRS-Hrhr/J
000673   HRS/J
001103   HRS/J-Hrhr Esdb/+ Esdb/J
002335   SKH2/J
000147   WLHR/LeJ
View Strains carrying   Hrhr     (5 strains)

Additional Web Information

Congenic Nomenclature

Research Applications

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

Immunology and Inflammation Research
CD Antigens, Antigen Receptors, and Histocompatibility Markers

Hrhr related

Cancer Research
Increased Tumor Incidence (Leukemia: lymphocytic)
Increased Tumor Incidence (Lymphomas: thymic)
Increased Tumor Incidence (Skin Cancers: Induced)
Toxicology

Cardiovascular Research
Diet-Induced Atherosclerosis (Relatively Resistant)

Dermatology Research
Skin and Hair Texture Defects

Immunology and Inflammation Research
Immunodeficiency Associated with Other Defects

Research Tools
Toxicology Research (drug/compound testing)

References

Additional References

Price and Supply Information

Strain Name: B6.A-H2-T18a.HRS-Hrhr/J
Stock Number: 001737

Price Details

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Supply Details

Standard SupplyRepository-Cryopreserved. Must Be Recovered. Please refer to the 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; Email: jaxservices@jax.org.

LicensingSee General Terms and Conditions below  
Control InformationView Control Information in Strain Details.

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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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