Strain Name: |
B6.C-H2bm1/ByBir-Gusbmps/BrkJ |
|---|---|
Stock Number: |
006559 |
Availability: | Repository-Cryopreserved |
Price and Supply Information | |
General Terms and Conditions |
| Genes & Alleles | Gusb; Gusbmps; H2-K; H2-Kbm1; H2; ; |
Type JAX® GEMM® Strain - Coisogenic Additional information on JAX® GEMM® Strains. Type JAX® GEMM® Strain - Congenic Type JAX® GEMM® Strain - Mutant Strain Type JAX® GEMM® Strain - Spontaneous Mutation Species laboratory mouse Generation F?+30pN1 Strain Description
Mice homozygous for the Gusbmps allele exhibit skeletal dysplasia as well as cognitive, hearing and visual deficits. Lifespan of the homozygotes is approximately six months. Homozygotes lack the lysomal enzyme, beta-glucoronidase, and, as a result, glycosaminoglycans accumulate in tissues throughout the body. Female homozygotes rarely conceive and do not lactate. This strain is a model for the human lysomal storage disease, mucopolysaccharidosis type VII.Strain Development
The Gusbmps mutation arose spontaneously on B6.C-H2bm1/By in 1976 (Birkenmeier et al., 1989).
Related Disease (OMIM) Terms |
Mammalian Phenotype Terms assigned by genotype |
| Allele Symbol | Gusbmps | ||
|---|---|---|---|
| Allele Name | beta glucuronidase, mucopolysaccharidosis VII | ||
| Common Name(s) | Gus-b; asd; gusmps; | ||
| Mutation Made By | Brian Soper, The Jackson Laboratory | ||
| Strain of Origin | C57BL/6By | ||
| Gene Symbol and Name | Gusb, glucuronidase, beta | ||
| Chromosome | 5 | ||
| Gene Common Name(s) | AI747421; Ac2-223; FLJ39445; Gur; Gus; Gus-r; Gus-s; Gus-t; Gus-u; Gut; MPS7; adipose storage deficiency; asd; beta-glucuronidase regulator; beta-glucuronidase structural; beta-glucuronidase systemic regulator; beta-glucuronidase temporal; expressed sequence AI747421; g; | ||
| Molecular Note | A 1-bp deletion creates a frameshift mutation within exon 10, which introduces a premature stop codon at codon 497. [MGI Ref ID J:13207] | ||
| Gene Symbol and Name | H2, histocompatibility-2, MHC | ||
| Chromosome | 17 | ||
| Gene Common Name(s) | H-2; MHC-II; | ||
| Allele Symbol | H2-Kbm1 | ||
| Allele Name | b haplotype mutation 1 | ||
| Common Name(s) | H(z1); H-2ba; H-2bm1; Kbm1; bm1; | ||
| Gene Symbol and Name | H2-K, histocompatibility 2, K region | ||
| Chromosome | 17 | ||
Strains carrying Gusbmps allele
006564 B6(C)-KitW-41J Gusbmps/BrkJ 000256 B6.C-H2bm1/ByBir-Gusbmps/J 006562 B6.CBy(Cg)-Gusbmps Gpi1a-m1J/BrkJ 006407 B6.Cg-Gusbmps/BrkJ 002086 B6.Cg-Gusbmps Tg(Gussx)1Wat/J 005053 NOD.Cg-Prkdcscid Gusbmps/SndsJ 001880 STOCK Gusbmps Tg(GUSB)4Sly/BirJ View Strains carrying Gusbmps (7 strains)
Strains carrying H2-Kbm1 allele
000368 B6.C-H2bm1/By 000256 B6.C-H2bm1/ByBir-Gusbmps/J 001060 B6.C-H2bm1/ByJ 006558 B6.Cg-H2bm1 Tg(GUSB)4Sly/SndsJ 002432 B6J x B6.C-H2bm1/ByJ-Cdh23v-J/J View Strains carrying H2-Kbm1 (5 strains)
Congenic Nomenclature
Gusbmps relatedDevelopmental Biology Research
Growth Defects Growth Defects (homozygous)
Metabolism Research
Mouse/Human Gene Homologs
mucopolysaccharidosis type VII, GUSB deficiency
Neurobiology Research
Behavioral and Learning Defects
Sensorineural Research
Developmental Biology Research
Growth Defects Growth Defects (homozygous)
Skeletal Defects
Metabolism Research
Mouse/Human Gene Homologs
mucopolysaccharidosis type VII, GUSB deficiency
Neurobiology Research
Behavioral and Learning Defects
Sensorineural Research
| Strain Name: | B6.C-H2bm1/ByBir-Gusbmps/BrkJ |
| Stock Number: | 006559 |
IMPORTANT NOTE: Prices are based on shipping destination. The shipping destinations are:
| Price(s) in US dollars ($) | |||||
|---|---|---|---|---|---|
| Cryorecovery Fee | $2470.00 | ||||
| Standard Supply | Repository-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. |
| Licensing | See General Terms and Conditions below |
Purchasing Information
JAX® Mice Orders
Surgical Services
Contact Information
Orders & Technical Support
Tel: 800.422.6423 or 207.288.5845
Fax: 207.288.6150
Technical Support Email Form