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Type Chromosome Aberration; Inversion; Additional information on Mice with Chromosomal Aberrations. Type Mutant Stock; Radiation Induced Mutation; Additional information on Genetically Engineered Mutant Mice. Species laboratory mouse Appearance
brown
Related Genotype: a/a Tyrp1b/Tyrp1b
black
Related Genotype: a/a Tyrp1b/+ or a/a +/+Description
The Uoxin homozygous phenotype has incomplete penetrance. While 63% of Uoxin homozygotes die by 12-14 days of age, those that live to adulthood generally live a normal breeding life span. Homozygous adults display chronic polyuria, increased serum BUN and creatinine levels, and hydronephrosis with a concomitant inflammatory response that is followed by glomerular and tubular dilation. (Cook et al., 2001.)
| Control | ||
|---|---|---|
| None Available | ||
| Considerations for Choosing Controls | ||
Inversions
View Inversions (48 strains)
Congenic Nomenclature
View Related Disease (OMIM) Terms
Related Disease (OMIM) Terms
Hyperuricemic Nephropathy, Familial Juvenile; HNFJ - Models with phenotypic similarity to human disease where etiologies are distinct.2
2 Human genes are associated with this disease. Orthologs of those genes do not appear in the mouse genotype(s).
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
Uoxin/Uoxin
involves: C57BL/6J * DBA/2J
- lethality-postnatal
- postnatal lethality (MGI Ref ID J:70677)
- 63% die postnatally at 12-14 days
- renal/urinary system phenotype
- abnormal kidney morphology (MGI Ref ID J:70677)
- abnormal renal glomerulus morphology (MGI Ref ID J:70677)
- develop glomerular dilation
- dilated renal tubules (MGI Ref ID J:70677)
- hydronephrosis (MGI Ref ID J:70677)
- develop hydronephrosis with a concomitant inflammatory response, followed by glomerular and tubular dilation
- abnormal urine chemistry (MGI Ref ID J:70677)
- surviving adults show urine sediment containing ammonium and potassium urate calculi
- polyuria (MGI Ref ID J:70677)
- surviving adults exhibit chronic polyuria, the urine sediment containing ammonium and potassium urate calculi
- homeostasis/metabolism phenotype
- abnormal urine chemistry (MGI Ref ID J:70677)
- surviving adults show urine sediment containing ammonium and potassium urate calculi
- increased blood urea nitrogen level (MGI Ref ID J:70677)
- increased circulating creatinine level (MGI Ref ID J:70677)
- immune system phenotype
- chronic inflammation (MGI Ref ID J:70677)
- develop hydronephrosis with a concomitant inflammatory response
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:Uoxin related
Developmental Biology Research
Internal/Organ Defects (kidney)
Postnatal Mortality (Homozygous)
Internal/Organ Research
Kidney Defects
| Allele Symbol | Uoxin | ||
|---|---|---|---|
| Allele Name | urate oxidase In(3)55Rk-induced | ||
| Allele Type | Radiation induced | ||
| Strain of Origin | DBA/2J | ||
| Gene Symbol and Name | Uox, urate oxidase | ||
| Chromosome | 3 | ||
| Gene Common Name(s) | AI663847; UOX-2; Uri; Uri2; expressed sequence AI663847; | ||
| General Note | See also In(3)55Rk-d and In(3)55Rk-p. | ||
| Molecular Note | PCR analysis on genomic DNA derived from mice carrying the In(3)55K inversion suggests that a disruption 3' to base 844 of exon 7 results in the mutation. Northern blot analysis on mRNA derived from liver RNA of homozygous mice confirmed that negligible amounts of encoded transcript was produced from this allele. [MGI Ref ID J:70677] | ||
| Gene Symbol and Name | In(3)55Rk-d, inversion, Chr 3, Roderick 55, distal | ||
| Chromosome | 3 | ||
| Gene Common Name(s) | In(3)55Rk; In55Rk; | ||
| Gene Symbol and Name | In(3)55Rk-p, inversion, Chr 3, Roderick 55, proximal | ||
| Chromosome | 3 | ||
| Gene Common Name(s) | In(3)55Rk; In55Rk; | ||
This strain will not have a genotyping protocol or one is not currently available.
Helpful Links
Optimizing PCR Protocols
Cook SA; Akeson EC; Calvano C; Johnson KR; Mandell J; Hawes NL; Bronson RT; Roderick TH; Davisson MT. 2001. Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene. Cytogenet Cell Genet 93(1-2):77-82. [PubMed: 11474184] [MGI Ref ID J:70677]
Cook S; Johnson K; Davisson M. 1997. The mouse urate oxidase gene, Uox, maps to distal chromosome 3. Mamm Genome 8(8):623-4. [PubMed: 9250879] [MGI Ref ID J:38316]
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 |
|
*Price(s) in US dollars ($)
Weeks of Age Price* Gender Cryorecovery Fee $1900.00
| Pricing for International shipping destinations |
|
*Price(s) in US dollars ($)
Weeks of Age Price* Gender Cryorecovery Fee $2470.00
| Standard Supply | Repository-Cryopreserved. Must Be Recovered. Please refer to pricing and supply notes for further information. |
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| Supply Notes |
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| Control | ||
|---|---|---|
| None Available | ||
| 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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| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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