Go to JAX® Mice Query Form

Strain Name:

C3A Pde6brd1.O20/A-Prph2Rd2/J

Stock Number:

001957

Availability:

Repository-Cryopreserved


Price and Supply Information

General Terms and Conditions

Former Name      C3A Pde6brd1.O20/A-RdsRd2/J    (Changed: 08-DEC-06 )
      C3A Pde6brd1.O20/A-Prph2Rd2    (Changed: 15-DEC-04 )
Genes & Alleles   Pde6b;   Pde6brd1;   Prph2;   Prph2Rd2;


Product Information

Strain Details

Type JAX® GEMM® Strain - Congenic
Additional information on JAX® GEMM® Strains.
Type JAX® GEMM® Strain - Mutant Strain
Specieslaboratory mouse

Important Note
See article "Genetic Background Effects: Can Your Mice See?", JAX Notes Spring 2002, No. 485.

Strain Development
This strain was developed in the laboratory of Dr. Willem J. De Grip at Erasmus Universiteit, Rotterdam, the Netherlands. Mice of strains homozygous for Prph2Rd2 and for Pde6brd1 were crossed to produce double heterozygotes; these F1 animals were then intercrossed, and mice homozygous for both mutations were selected from the F2 for further breeding. The Pde6brd1 strain used was derived from an intercross following 8 generations of backcrossing the wild type Pde6b allele from C57BL/LiA onto the C3Hf/HeA background; this homozygous Pde6brd1/Pde6brd1 line was the partner strain of the homozygous Pde6b wildtype strain C3A.BLiA-+Pdeb (Stock No. 001912), derived from the same intercross. The latter was the parent strain of the Prph2Rd2 strain, C3HeA.BLiA-+Pde6b.O20A-Prph2Rd2 (see Stock No. 001979), used in the initial cross leading to the present strain (Schalken et al. 1990; S. Sanyal, personal communication). Thus, the background of Stock No. 001957 is primarily C3Hf/HeA, but small regions of the genome may be derived from O20/A and/or from C57BL/LiA.

Mammalian Phenotype Terms assigned by genotype

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

Pde6brd1/Pde6brd1 Prph2Rd2/Prph2Rd2

        either: C.Cg-Pde6brd1 Prph2Rd2 or C3.Cg-Pde6brd1 Prph2Rd2
  • vision/eye phenotype
  • abnormal Muller cell morphology (MGI Ref ID J:27850)
    • increase in density of Muller cells and fibers is intermediate compared to the single homozygotes
  • absent photoreceptor outer segment (MGI Ref ID J:27850)
    • remaining photoreceptor cells lack outer segments
  • retinal photoreceptor degeneration (MGI Ref ID J:27850)
    • the rate of photoreceptor loss is slower than in Pde6brd1 single homozygotes
  • nervous system phenotype
  • abnormal Muller cell morphology (MGI Ref ID J:27850)
    • increase in density of Muller cells and fibers is intermediate compared to the single homozygotes
  • absent photoreceptor outer segment (MGI Ref ID J:27850)
    • remaining photoreceptor cells lack outer segments
  • retinal photoreceptor degeneration (MGI Ref ID J:27850)
    • the rate of photoreceptor loss is slower than in Pde6brd1 single homozygotes

Gene & Allele Details

Allele Symbol Pde6brd1
Allele Name retinal degeneration 1
Common Name(s) rd; rd-1; rd1; rodless retina;
Gene Symbol and Name Pde6b, phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide
Chromosome 5
Gene Common Name(s) CSNB3; PDEB; Pdeb; RP40; nmf137; phosphodiesterase, cGMP, rod receptor, beta polypeptide; r; rd; rd-1; rd1; rd10; retinal degeneration; retinal degeneration 1; retinal degeneration 10;
Molecular Note Two mutations have been identified in rd1 mice. A murine leukimia virus (Xmv-28) insertion in reverse orientation in intron 1 is found in all mouse strains with the rd1 phenotype. Further, a nonsense mutation (C to A transversion) in codon 347 that results in a truncation eliminating more than half of the predicted encoded protein, including the catalytic domain has also been identified in all rd1 strains of mice. A specific degradation of mutant transcript during or after pre-mRNA splicing is suggested. [MGI Ref ID J:11513] [MGI Ref ID J:4366] [MGI Ref ID J:51361]
 
Allele Symbol Prph2Rd2
Allele Name retinal degeneration 2
Common Name(s) Prph2Rds; Rd-2; Rds; RdsRd2; rds-; retinal degeneration slow;
Strain of OriginO20/A
Gene Symbol and Name Prph2, peripherin 2
Chromosome 17
Gene Common Name(s) AOFMD; AVMD; PRPH; RDS; RP7; RSRDS; Rd-2; Rd2; Rds; TSPAN22; retinal degeneration 2; retinal degeneration, slow; retinal degeneration, slow (retinitis pigmentosa 7);
General Note The rate of retinal degeneration in mutants doubly homozygous for two retinal degeneration mutations (Pde6brd1 and RdsRd2) is intermediate between those of the two homozygotes (J:12044). The double homozygote shows an intermediate level of mRNAs for the beta subunit of cGMP-PDE and for several other phototransduction related proteins, suggesting an interaction between Pde6brd1 and RdsRd2 (J:2579).
Molecular Note The mutation is an insertion of approximately 10 kb in the gene after nucleotide 899 (numbering of the encoded mRNA), disrupting the protein coding sequence in exon 2. The inserted DNA was similar to both the TSE of mice, repeated elements found in the H2 complex, and to the mouse early transposon (ETn). Northern blot analysis demonstrated that an aberrant 12 kb transcript was produced from this allele, although at reduced levels compared to wild type. This allele is predicted to encode a truncated protein with its carboxy terminal 116 amino acids replaced by 35 amino acids from sequences in the insertion. [MGI Ref ID J:9635]

Control Information

   
   Control for Pde6brd1 alone: C3HeA.BLiA-+Pde6b.020-RdsRd2 (Stock No. 001979)

Control for RdsRd2 alone: C3H/HeJ (Stock No. 000659)

 
  Considerations for Choosing Controls
  Control Pricing Information for JAX® GEMM® Strains

Related Strains

Strains carrying   Pde6brd1 allele
004202   B6.C3 Pde6brd1 Hps4le/+ +-Lmx1adr-8J/J
000002   B6.C3-Pde6brd1 Hps4le/J
001022   B6C3FeF1/J a/a
000652   BDP/J
000653   BUB/BnJ
002439   C3.129P2(B6)-B2mtm1Unc/J
005494   C3.129S1(B6)-Grm1rcw/J
000480   C3.MRL-Faslpr/J
005973   C3Bir.129P2(B6)-Il10C3Bir/LtJ
004326   C3Bir.129P2(B6)-Il10tm1Cgn/Lt
003968   C3Bir.129P2(B6)-Il10tm1Cgn/LtJ
001906   C3Ga.Cg-Catb/J
001904   C3H-Atcayji-hes/J
000659   C3H/HeJ
000784   C3H/HeJ-Faslgld/J
000509   C3H/HeJ-Lystbg-2J/J
002433   C3H/HeJ-Spnb4qv-lnd2J/J
005972   C3H/HeJBirLtJ
001824   C3H/HeJSxJ
000635   C3H/HeOuJ
000474   C3H/HeSn
001431   C3H/HeSn-ocd/J
000661   C3H/HeSnJ
002235   C3H/HeSnJ-Ctnna2cdf/J
002333   C3H/HeSnJ-gri/J
006435   C3HeB.SW-Soaa/MonJ
000658   C3HeB/FeJ
001576   C3HeB/FeJ-Atp7btx-J/J
002588   C3HeB/FeJ-Eya1bor/J
001533   C3HeB/FeJ-Mc1rE-so Gli3Xt-J/J
001886   C3HeB/FeJLe a/a-gnd/J
001908   C3HfB/BiJ
001502   C3Sn.B6-Epha4rb/J
001547   C3Sn.Cg-Cm/J
000656   CBA/J
000813   CBA/J-Atp7aMo-pew/J
000660   DA/HuSnJ
000023   FL/1ReJ
000025   FL/4ReJ
003024   FVB.129P2(B6)-Fmr1tm1Cgr/J
002539   FVB.129P2-Abcb4tm1Bor/J
002935   FVB.129S2(B6)-Ccnd1tm1Wbg/J
002953   FVB.Cg-Tg(MMTVTGFA)254Rjc/J
003170   FVB.Cg-Tg(Myh6-tTA)6Smbf/J
003078   FVB.Cg-Tg(WapIgf1)39Dlr/J
003257   FVB/N-Tg(GFAPGFP)14Mes/J
002374   FVB/N-Tg(MMTV-PyVT)634Mul/J
002856   FVB/N-Tg(TIE2-lacZ)182Sato/J
002384   FVB/N-Tg(UcpDta)1Kz/J
001800   FVB/NJ
003487   FVB/NJ-Tg(XGFAP-lacZ)3Mes/J
001491   FVB/NMob
000734   MOLD/RkJ
000550   MOLF/EiJ
002423   NON/ShiLtJ
000679   P/J
000680   PL/J
100299   PLSJLF1/J
000269   SB/LeJ
005651   SJL.AK-Thy1a/TseJ
000686   SJL/J
000688   ST/bJ
004808   STOCK Mapttm1(EGFP)Klt Tg(MAPT)8cPdav/J
002648   STOCK a/a Cln6nclf/J
000279   STOCK gr +/+ Ap3d1mh/J
005965   STOCK Tg(Pomc1-cre)16Lowl/J
004770   SW.B6-Soab/J
002023   SWR.M-Emv21 Emv22/J
000689   SWR/J
000939   SWR/J-Clcn1adr-mto/J
000692   WB/ReJ KitW/J
100410   WBB6F1/J-KitW/KitW-v/J
000693   WC/ReJ KitlSl/J
100401   WCB6F1/J KitlSl KitlSl-d
View Strains carrying   Pde6brd1     (74 strains)

Strains carrying   Prph2Rd2 allele
001979   C3A.BLiA-Pde6b+.O20-Prph2Rd2/J
001981   O20/A-Prph2Rd2/J
View Strains carrying   Prph2Rd2     (2 strains)

View Strains carrying other alleles of Pde6b     (8 strains)

Additional Web Information

Congenic Nomenclature
JAX Notes, Spring 2002; 485. Genetic Background Effects: Can Your Mice See?

Research Applications

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

Pde6brd1 related

Mouse/Human Gene Homologs
retinitis pigmentosa, autosomal recessive

Sensorineural Research
Retinal Degeneration

Prph2Rd2 related

Mouse/Human Gene Homologs
retinal degeneration, slow

Research Tools
Sensorineural Research (retinal degeneration)

Sensorineural Research
Retinal Degeneration

References

Selected Reference(s)

Schalken JJ; Janssen JJ; Sanyal S; Hawkins RK; de Grip WJ. 1990. Development and degeneration of retina in rds mutant mice: immunoassay of the rod visual pigment rhodopsin. Biochim Biophys Acta 1033(1):103-9. [PubMed: 2137350]  [MGI Ref ID J:109932]

Additional References

Price and Supply Information

Strain Name: C3A Pde6brd1.O20/A-Prph2Rd2/J
Stock Number: 001957

Price Details

IMPORTANT NOTE: Prices are based on shipping destination. The shipping destinations are:

*Pricing for Shipping Destination selected:

        USA, Canada and Mexico

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

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; Email: jaxservices@jax.org.

LicensingSee General Terms and Conditions below  
Control InformationView Control Information in Strain Details.
View Control Pricing Information for JAX® Strains.

General Terms and Conditions

View JAX® Mice & Services Conditions of Use.

The Jackson Laboratory's Genotype Promise

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.
Ordering and Purchasing Information

      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

Go to JAX® Mice Query Form

(2.15)