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Strain Name: |
B6;129-Crb1rd8/J |
Stock Number: |
004852 |
Availability:
| Repository-Cryopreserved |
| Former Name |
B6;129-Crb1rd8-nmf144/J (Changed: 15-DEC-04
)
|
|
NMF144 (Changed: 15-DEC-04
)
|
| Genes & Alleles |
Crb1;
Crb1rd8;
|
Product Information
Strain Details
| Type |
JAX® GEMM® Strain -
Chemically Induced Mutation |
| Additional information on
JAX® GEMM® Strains. |
| Type |
JAX® GEMM® Strain -
Coisogenic |
| Type |
JAX® GEMM® Strain -
Mutant Strain |
| Species | laboratory mouse |
| Background Strain |
C57BL/6J
|
| Donor Strain |
129
|
| H2 Haplotype | b |
| Generation | N3F2N1p
(23-JUL-04)
|
|
|
Strain Description
View strain phenotype and additional information on the Neuroscience Mutagenesis Facility web page for Crb1rd8 (Crb1nmf144) entry.
Mammalian Phenotype Terms assigned by genotype
The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.
Crb1rd8/Crb1rd8
STOCK Crb1rd8/J
- vision/eye phenotype
- abnormal ocular fundus morphology
(J:85459)
- mice exhibit large, irregularly shaped spots concentrated in the inferior nasal quadrant of the fundus as early as week 3 that correspond to retinal folds and pseudorosettes
- abnormal retina morphology
(J:85459)
- retinal thinning in both the inner and outer segment is observed
- the external limiting membrane in the retina is fragmented and disorganized at 2 weeks and is more severe at 4 weeks
- abnormal Muller cell morphology
(J:85459)
- Muller cells exhibit increased electron density and cytoplasmic strands that are more easily traced through the plexiform layer than in wild type mice
- abnormal retinal photoreceptor morphology
(J:85459)
- the photoreceptor lamellae breaks down
- abnormal photoreceptor inner segment morphology
(J:85459)
- the photoreceptor inner segments lose their orderly arrangement
- by 5 months the inner segment approaches the retinal pigment epithelium
- swelling occurs in portions of the inner segments
- short photoreceptor inner segment
(J:85459)
- at 4 weeks the photoreceptor inner segments are 25% shorter
- decreased retinal photoreceptor cell number
(J:85459)
- in the region of focal degeneration photoreceptors are lost
- photoreceptor outer segment degeneration
(J:85459)
- by week 10 the outer segment begins to fragment
- by 5 months only a few outer segment fragments remain
- short photoreceptor outer segment
(J:85459)
- the photoreceptor outer segments are shortened
- thin retinal outer nuclear layer
(J:85459)
- in older mice, the retinal outer nuclear layer is reduced to a single row of nuclei
- nervous system phenotype
- abnormal Muller cell morphology
(J:85459)
- Muller cells exhibit increased electron density and cytoplasmic strands that are more easily traced through the plexiform layer than in wild type mice
- abnormal retinal photoreceptor morphology
(J:85459)
- the photoreceptor lamellae breaks down
- abnormal photoreceptor inner segment morphology
(J:85459)
- the photoreceptor inner segments lose their orderly arrangement
- by 5 months the inner segment approaches the retinal pigment epithelium
- swelling occurs in portions of the inner segments
- short photoreceptor inner segment
(J:85459)
- at 4 weeks the photoreceptor inner segments are 25% shorter
- decreased retinal photoreceptor cell number
(J:85459)
- in the region of focal degeneration photoreceptors are lost
- photoreceptor outer segment degeneration
(J:85459)
- by week 10 the outer segment begins to fragment
- by 5 months only a few outer segment fragments remain
- short photoreceptor outer segment
(J:85459)
- the photoreceptor outer segments are shortened
Crb1rd8/Crb1rd8
involves: C3HfB6/Ga * C57BL/6 * CAST/EiJ
- vision/eye phenotype
- abnormal retina morphology
(J:85459)
- 19% of mice do not display the spotting phenotype on a CAST/EiJ mixed background
Crb1rd8/Crb1rd8
B6.Cg-Crb1rd8
- vision/eye phenotype
- *normal* vision/eye phenotype
(J:85459)
- mice no longer display the spotting phenotype when backcrossed from a CAST/EiJ background onto a C57BL/6 background
|
Gene & Allele Details
| Allele Symbol |
Crb1rd8 |
| Allele Name |
retinal degeneration 8 |
| Common Name(s) |
nmf144;
|
| Strain of Origin | C57BL/6J |
| Gene Symbol and Name |
Crb1, crumbs homolog 1 (Drosophila) |
| Chromosome |
1 |
| Gene Common Name(s) |
7530426H14Rik;
A930008G09Rik;
LCA8;
RIKEN cDNA 7530426H14 gene;
RIKEN cDNA A930008G09 gene;
RP12;
|
| Molecular Note |
The mutation in the rd8 mouse has been identified as a single base deletion in the Crb1 gene. This deletion causes a frame shift and a premature stop codon that truncates the transmembrane and cytoplasmic domain of the protein. [J:85459]
|
Control Information
Related Strains
Strains carrying Crb1rd8 allele
View Strains carrying Crb1rd8 (1 strain)
Research Applications
This mouse can be used to support research in many areas including:
Neurobiology Research
Neuroscience Mutagenesis Facility Strain
Crb1rd8 related
Cell Biology Research
Defects in Cell Adhesion Molecules
Developmental Biology Research
Eye Defects
Mouse/Human Gene Homologs
Retinitis pigmentosa 12; Leber congenital amaurosis (CLA)
Sensorineural Research
Retinal Degeneration
References
Selected Reference(s)
Mehalow AK; Kameya S; Smith RS; Hawes NL; Denegre JM; Young JA; Bechtold L; Haider NB; Tepass U; Heckenlively JR; Chang B; Naggert JK; Nishina PM. 2003. CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina. Hum Mol Genet
12(17):2179-89.
[PubMed: 12915475]
[J:85459]
Additional References
Price and Supply Information
| Strain Name: |
B6;129-Crb1rd8/J |
| Stock Number: |
004852 |
Price Details
IMPORTANT NOTE: Prices are based on shipping destination.
To view prices, select your shipping destination.
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Supply Details
| Standard Supply | Repository-Cryopreserved. Must Be Recovered. Please refer to the 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.
This strain is included in the Neuroscience Mutagenesis Facility (NMF).
|
| Licensing | See General Terms and Conditions below
|
| Control Information | View Control Information in Strain Details.
|
|---|
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JAX® Mice & Services Conditions of Use.
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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.
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