Type Congenic; Mutant Strain; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Additional information on Congenic nomenclature. Mating System Sibling x Sibling (Female x Male) 01-MAR-06 Species laboratory mouse Background Strain C3H/HeA Donor Strain C57BL/LiA Appearance
agouti
Related Genotype: A/ADescription
In this congenic strain, the wild type Pde6b allele from C57BL/LiA was introgressed onto the C3Hf/HeA background. Retinal degeneration 1 (Pde6brd1) is a spontaneous mutation that is present in multiple inbred strains, including the C3H substrains. Strains that carry rd1 lack rod cells. This strain provides a sighted C3H mouse for use in research studies that require normal vision.Development
This strain was developed in the laboratory of Willem J. de Grip at Erasmus Universiteit, Rotterdam, the Netherlands. An initial cross of C3Hf/HeA with C57BL/LiA was followed by 8 generations of backcrossing to C3Hf/HeA to introgress the wild type Pde6b allele of C57BL/LiA onto the C3Hf/HeA background. The heterozygous progeny of the last backcross were intercrossed to produce homozygous wild type (Pde6b+/Pdeb+) mice, after which the strain was maintained by sib inbreeding. The strain had exceeded 30 generations of sibling mating when it was sent to The Jackson Laboratory in 1991. (Schalken et al., 1990 and TJL documentation)Additional backgrounds available: using this strain as the donor, the wild type allele of Pde6b was backcrossed for 10 generations to C3H/HeSnJ. This was done for the purpose of generating a hardier control/background strain for use in studies of additional retinal degeneration mutations. The product of this backcross, C3Sn.BLiA-Pde6b+/Dn (Stock No. 003648), is now maintained by sib mating.
| Control | ||
|---|---|---|
| See control note: | This strain can be used as a normal, sighted control for C3A Pde6brd1.O20-RdsRd2 (001957) and for C3A.BLiA-+Pde6b.O20-RdsRd2 (001979). For applications related to Pde6brd1, this strain serves as a control for C3H/HeJ (000659). | |
| Considerations for Choosing Controls | ||
Strains carrying Pde6b+ allele
005252 B6EiC3Sn.BLiA-Ts(1716)65Dn/DnJ 003647 B6EiC3Sn.BLiAF1/J 002802 C3.BLiA Pde6b+-Krd/J 001979 C3A.Cg-Pde6b+ Prph2Rd2/J 003648 C3Sn.BLiA-Pde6b+/DnJ 004624 FVB.129P2-Pde6b+ Tyrc-ch Fmr1tm1Cgr/J 004828 FVB.129P2-Pde6b+ Tyrc-ch/AntJ 004808 STOCK Mapttm1(EGFP)Klt Tg(MAPT)8cPdav/J View Strains carrying Pde6b+ (8 strains)
Strains carrying other alleles of Pde6b
004202 B6.C3 Pde6brd1 Hps4le/+ +-Lmx1adr-8J/J 000002 B6.C3-Pde6brd1 Hps4le/J 004297 B6.CXB1-Pde6brd10/J 001022 B6C3FeF1/J a/a 000652 BDP/J 000653 BUB/BnJ 002439 C3.129P2(B6)-B2mtm1Unc/J 005494 C3.129S1(B6)-Grm1rcw/J 000509 C3.Cg-Lystbg-2J/J 000480 C3.MRL-Faslpr/J 001957 C3A Pde6brd1.O20/A-Prph2Rd2/J 005973 C3Bir.129P2(B6)-Il10C3Bir/LtJ 004326 C3Bir.129P2(B6)-Il10tm1Cgn/Lt 003968 C3Bir.129P2(B6)-Il10tm1Cgn/LtJ 006435 C3Fe.SW-Soaa/MonJ 001904 C3H-Atcayji-hes/J 000659 C3H/HeJ 000511 C3H/HeJ-Ap3d1mh-2J/J 000784 C3H/HeJ-Faslgld/J 002433 C3H/HeJ-Sptbn4qv-lnd2J/J 005972 C3H/HeJBirLtJ 001824 C3H/HeJSxJ 000635 C3H/HeOuJ 000474 C3H/HeSn 001431 C3H/HeSn-ocd/J 000661 C3H/HeSnJ 002333 C3H/HeSnJ-gri/J 001576 C3He-Atp7btx-J/J 000658 C3HeB/FeJ 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/EiGrsrJ 002235 C3Sn.C3-Ctnna2cdf/J 001547 C3Sn.Cg-Cm/J 001906 C3fBAnl.Cg-Catb/AnlJ 004766 C57BL/6J-Pde6brd1-2J/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 003487 FVB.Cg-Tg(XGFAP-lacZ)3Mes/J 003257 FVB/N-Tg(GFAPGFP)14Mes/J 002856 FVB/N-Tg(TIE2-lacZ)182Sato/J 002384 FVB/N-Tg(UcpDta)1Kz/J 001800 FVB/NJ 001491 FVB/NMob 000734 MOLD/RkJ 000550 MOLF/EiJ 002423 NON/ShiLtJ 000679 P/J 000680 PL/J 000269 SB/LeJ 010968 SB;C3Sn-Lrp4mdig-2J/GrsrJ 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-d/J)F1-KitlSl/KitlSl-d/J View Strains carrying other alleles of Pde6b (77 strains)
View Research Applications
Currently there is no phenotype information for this strain.Research Applications
This mouse can be used to support research in many areas including:Pde6b+ related
Mouse/Human Gene Homologs
retinitis pigmentosa, wildtype
Sensorineural Research
Retinal Degeneration
wild-type
| Allele Symbol | Pde6b+ | ||
|---|---|---|---|
| Allele Name | wild type | ||
| Allele Type | Not Applicable | ||
| Mutation Made By | Frank Kooy, University of Antwerp | ||
| Gene Symbol and Name | Pde6b, phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide | ||
| Chromosome | 5 | ||
| Gene Common Name(s) | CSNB3; CSNBAD2; PDEB; Pdeb; RP40; nmf137; phosphodiesterase, cGMP, rod receptor, beta polypeptide; r; rd; rd-1; rd1; rd10; retinal degeneration; retinal degeneration 1; retinal degeneration 10; | ||
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]
Pde6b+ relatedDobkin C; Rabe A; Dumas R; El Idrissi A; Haubenstock H; Brown WT. 2000. Fmr1 knockout mouse has a distinctive strain-specific learning impairment. Neuroscience 100(2):423-9. [PubMed: 11008180] [MGI Ref ID J:119166]
Ivanco TL; Greenough WT. 2002. Altered mossy fiber distributions in adult Fmr1 (FVB) knockout mice. Hippocampus 12(1):47-54. [PubMed: 11918288] [MGI Ref ID J:113177]
Sakamoto K; McCluskey M; Wensel TG; Naggert JK; Nishina PM. 2009. New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene. Hum Mol Genet 18(1):178-92. [PubMed: 18849587] [MGI Ref ID J:142108]
Zhao MG; Toyoda H; Ko SW; Ding HK; Wu LJ; Zhuo M. 2005. Deficits in trace fear memory and long-term potentiation in a mouse model for fragile X syndrome. J Neurosci 25(32):7385-92. [PubMed: 16093389] [MGI Ref ID J:100197]
Animal Health Reports
Room Number A1
Colony Maintenance
Breeding & Husbandry Malocclusion occurs occasionally in this strain. Mating System Sibling x Sibling (Female x Male) 01-MAR-06
| Pricing for USA, Canada and Mexico shipping destinations |
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Price per mouse (US dollars $) Gender Genotypes Provided Individual Mouse $109.30 Female or Male Homozygous for Pde6b+ Standard Supply
Research Strain. Availability determined by The Jackson Laboratory scientist holding the strain.
| Pricing for International shipping destinations |
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Price per mouse (US dollars $) Gender Genotypes Provided Individual Mouse $142.10 Female or Male Homozygous for Pde6b+ Standard Supply
Research Strain. Availability determined by The Jackson Laboratory scientist holding the strain.
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Research Strain. Availability determined by The Jackson Laboratory scientist holding the strain.
| Control | ||
|---|---|---|
| See control note: | This strain can be used as a normal, sighted control for C3A Pde6brd1.O20-RdsRd2 (001957) and for C3A.BLiA-+Pde6b.O20-RdsRd2 (001979). For applications related to Pde6brd1, this strain serves as a control for C3H/HeJ (000659). | |
| Considerations for Choosing Controls | ||
| Control Pricing Information for Genetically Engineered Mutant Strains. | ||
| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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