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Former Names SWR.M-Emv21/22 (Changed: 15-DEC-04 ) Type Congenic; Mutant Strain; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Additional information on Congenic nomenclature. Species laboratory mouse Donor Strain MEV/Ty H2 Haplotype q Generation N7F16 Appearance
albino
Related Genotype: Tyrc/TyrcImportant Note
This strain is homozygous for Pde6brd1, which causes early-onset retinal degeneration.Description
This strain carries a pair of linked retroviral insertions that occurred simultaneously on Chr 18 in a MEV substrain related to MEV/1Ty. Homozygosity for one of the insertions causes a juvenile lethal wasting condition that results in death at approximately 16 days of age. The proviruses rarely recombine; during development of this incipient congenic strain, a mouse was never found to have Emv21 in the absence of Emv22. There is no evidence that either of these viruses causes germline or somatic infection resulting in integration of new germline copies. (brs per personal communication from B. Taylor)Development
SWR/J was made congenic for a pair of linked retroviral insertions, identified as Emv21 and Emv22, in the laboratory of Dr. Benjamin Taylor by an initial cross to a strain closely related to MEV/1Ty followed by backcrossing of progeny at the N1 and subsequent generations to SWR/J for 6 generations (to N7). Siblings from the final backcross were then intercrossed to make the strain homozygous, after which it was maintained by brother-sister inbreeding.
Strains carrying Pde6brd1 allele
View Strains carrying Pde6brd1 (74 strains)
Strains carrying other alleles of Pde6b
004297 B6.CXB1-Pde6brd10/J 005252 B6EiC3Sn.BLiA-Ts(1716)65Dn/DnJ 003647 B6EiC3Sn.BLiAF1 002802 C3.BLiA Pde6b+-Krd/J 001979 C3A.BLiA-Pde6b+.O20-Prph2Rd2/J 001912 C3A.BLiA-Pde6b+/J 003648 C3Sn.BLiA-Pde6b+/Dn 004766 C57BL/6J-Pde6brd1-2J/J 004828 FVB.129P2-Pde6b+ Tyrc-ch/AntJ 004808 STOCK Mapttm1(EGFP)Klt Tg(MAPT)8cPdav/J View Strains carrying other alleles of Pde6b (10 strains)
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
Pde6brd1 relatedDevelopmental Biology Research
Perinatal Lethality
Homozygous
Research Tools
Genetics Research
Gene Mapping
Virology Research
Linkage Testing Stock
Mouse/Human Gene Homologs
retinitis pigmentosa, autosomal recessive
Sensorineural Research
Retinal Degeneration
| Gene Symbol and Name | Emv22, endogenous ecotropic MuLV 22 | ||
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| Chromosome | 19 | ||
| Gene Common Name(s) | Emv-22; | ||
| Gene Symbol and Name | Emv21, endogenous ecotropic MuLV 21 | ||
| Chromosome | 18 | ||
| Gene Common Name(s) | Emv-21; | ||
| Allele Symbol | Pde6brd1 | ||
| Allele Name | retinal degeneration 1 | ||
| Allele Type | Spontaneous | ||
| Common Name(s) | Pdebrd1; rd; rd-1; rd1; rodless retina; | ||
This strain will not have a genotyping protocol or one is not currently available.
Helpful Links
Genotyping resources and troubleshooting
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 |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $1900.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
| Pricing for International shipping destinations |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $2470.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
| Standard Supply | Cryopreserved. Ready for recovery. Please refer to pricing and supply notes for further information. |
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| Supply Notes |
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| Important Note | |
| This strain is homozygous for Pde6brd1, which causes early-onset retinal degeneration. | |
Purchasing Information
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Technical Support Email Form
| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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