Strain Name: |
C3.129S1(B6)-Grm1rcw/J |
|---|---|
Stock Number: |
005494 |
Availability: | Repository-Cryopreserved |
Price and Supply Information | |
General Terms and Conditions |
| Former Name |
C3.129S1(B6)-rcw/J (Changed: 14-DEC-07
) |
| Genes & Alleles | Cdh23; Cdh23ahl; Grm1; Grm1rcw; Pde6b; Pde6brd1; |
Type JAX® GEMM® Strain - Congenic Additional information on JAX® GEMM® Strains. Type JAX® GEMM® Strain - Mutant Strain Type JAX® GEMM® Strain - Spontaneous Mutation Species laboratory mouse Background Strain C3H (see Development Field) Donor Strain 129S1/SvImJ H2 Haplotype k Important Note
This strain is homozygous for the retinal degeneration mutation Pde6brd1; it may also carry the age related hearing loss mutation, Cdh23ahl, which is linked to rcw within ~20 - 30 cM on Chr 10.Strain Description
Visibly, Grm1rcw/Grm1rcw mice are identifiable by 2.5 - 3 weeks of age. Their constant wobbly gait frequently throws them off balance, but only briefly, as they show immediate and normal righting response. When walking, they often brace for balance with their fore- and hindfeet extended forward or sideways. Their heads lurch mildly and the mutants often sit on their haunches when motion falters. Their forefeet show normal grip strength when the mutant mice are pulled gently backwards over a cage cover. When picked up by the tail, they may clasp their hindfeet. However, they show sufficient hindlimb strength to prevent their falling when placed on an edge. Mutants live through adulthood, and mice of both sexes breed. Grm1rcw has been mapped between the flanking markers D10Mit49, at map position 6.3 Mb and D10Mit80, at map position 11.4 Mb.Strain Development
rcw arose in the 129S1/SvImJ production colony at The Jackson Laboratory in 1998. An affected female was crossed to a C3HeB/FeJ male, and the stock was then maintained by sib matings for seven generations. It was then decided to transfer rcw onto C3FeLe.B6-a/a so that females of an agouti C3H subline could serve as ovarian transplant hosts if ovarian transplantation should prove necessary to maintain the mutation on an inbred background. The resulting strain was named C3FeLe.Cg a-rcw/J. This strain is no longer available. The homozygous mutant phenotype did not diminish or show reduced viability at N5. In 2005 embryos were generated for cryopreservation using C3HeB/FeJ agouti females and congenic C3FeLe.B6-a/a homozygous mutant males and were assigned stock#5494 and named C3.Cg-rcw/J. This thawed strain will be segregating for a and A.
Mammalian Phenotype Terms assigned by genotype |
| Allele Symbol | Grm1rcw | ||
|---|---|---|---|
| Allele Name | recoil wobbler | ||
| Strain of Origin | 129S1/SvImJ | ||
| Gene Symbol and Name | Grm1, glutamate receptor, metabotropic 1 | ||
| Chromosome | 10 | ||
| Gene Common Name(s) | G protein coupled receptor, family C, group 1, member A; G protein-coupled receptor, family C, group 1, member A; GPRC1A; GRM1A; Gprc1a; MGLUR1; MGLUR1A; mGlu1; neuroscience mutagenesis facility, 373; nmf373; rcw; recoil wobbler; wobbles; wobl; | ||
| Molecular Note | A spontaneous mutation that arose at The Jackson Laboratory. A G1251T transversion causing an E292D amino acid change has been identified. [MGI Ref ID J:127311] | ||
| Allele Symbol | Cdh23ahl | ||
| Allele Name | age related hearing loss 1 | ||
| Common Name(s) | Cdh23753A; mdfw; | ||
| Allele Symbol | Pde6brd1 | ||
| Allele Name | retinal degeneration 1 | ||
| Common Name(s) | rd; rd-1; rd1; rodless retina; | ||
Strains carrying Cdh23ahl allele
001137 129P1/ReJ 000690 129P3/J 002065 129T2/SvEmsJ 000691 129X1/SvJ 000646 A/J 000647 A/WySnJ 003070 ALR/LtJ 003072 ALS/LtJ 004502 B6;AKR-Lxl2/J 001026 BALB/cByJ 000653 BUB/BnJ 000664 C57BL/6J 004764 C57BL/6J-Cdh23v-8J/J 003129 C57BL/6J-Epha4rb-2J/J 004820 C57BL/6J-Kcne12J/J 004703 C57BL/6J-Kcnq2Nmf134/J 004811 C57BL/6J-nmf110/J 004812 C57BL/6J-nmf111/J 004747 C57BL/6J-nmf118/J 004656 C57BL/6J-nmf88/J 004391 C57BL/6J-Chr 13A/J/NaJ 004385 C57BL/6J-Chr 7A/J/NaJ 000662 C57BLKS/J 000667 C57BR/cdJ 000668 C57L/J 000669 C58/J 000657 CE/J 000670 DBA/1J 001140 DBA/1LacJ 000671 DBA/2J 007048 DBA/2J-Gpnmb+/SjJ 002106 KK/HlJ 000675 LG/J 000676 LP/J 000677 MA/MyJ 001976 NOD/ShiLtJ 002050 NOR/LtJ 000679 P/J 002747 SENCARB/PtJ 002335 SKH2/J 003392 STOCK Crb1rd8/J View Strains carrying Cdh23ahl (41 strains)
Strains carrying Pde6brd1 allele
View Strains carrying Pde6brd1 (74 strains)
Strains carrying other alleles of Cdh23
008288 B6(Cg)-Cdh23v-11J/J 002756 B6.CAST-Cdh23Ahl+/Kjn 002432 B6J x B6.C-H2bm1/ByJ-Cdh23v-J/J 002552 C57BL/6J-Cdh23v-2J/J 004764 C57BL/6J-Cdh23v-8J/J 004819 C57BL/6J-Cdh23v-9J/J 005016 CByJ;B6-Cdh23v-10J/J 000275 V/LeJ View Strains carrying other alleles of Cdh23 (8 strains)
Strains carrying other alleles of Grm1
005814 B6.129P2-Grm1tm1Dgen/J 005561 C57BL/6J-Grm1nmf373/J 005521 C57BL/6J-Grm1rcw-3J/J View Strains carrying other alleles of Grm1 (3 strains)
Strains carrying other alleles of Pde6b
004297 B6.CXB1-Pde6brd10/J 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 (8 strains)
Congenic Nomenclature
Cdh23ahl related
Grm1rcw relatedNeurobiology Research
Vestibular and Hearing Defects (Age related hearing loss)
Sensorineural Research
Vestibular and Hearing Defects (Age related hearing loss)
Pde6brd1 relatedNeurobiology Research
Ataxia (Movement) Defects
Mouse/Human Gene Homologs
retinitis pigmentosa, autosomal recessive
Sensorineural Research
Retinal Degeneration
| Strain Name: | C3.129S1(B6)-Grm1rcw/J |
| Stock Number: | 005494 |
IMPORTANT NOTE: Prices are based on shipping destination. The shipping destinations are:
| Price(s) in US dollars ($) | |||||
|---|---|---|---|---|---|
| Cryorecovery Fee | $1900.00 | ||||
| Cryopreserved Embryos Fee | $1600.00 | ||||
| Standard Supply | Repository-Cryopreserved. Must Be Recovered. Please refer to the Supply Notes for further information. |
|---|---|
| Supply Notes |
Cryopreserved Embryos This strain is also available as cryopreserved embryos from our Repository. Orders for cryopreserved embryos are supplied subject to a signed agreement that must be returned to the Customer Service Department after order placement. Experienced technicians at The Jackson Laboratory have recovered frozen embryos of this strain successfully. We will provide you enough embryos to perform two embryo transfers. The Jackson Laboratory does not guarantee successful recovery at your facility. For complete information on purchasing embryos from our repository, please visit our Cryopreserved Embryos web page. 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 |
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