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Type Mutant Strain; Spontaneous Mutation; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Species laboratory mouse Generation N37 F1 Appearance
dark grey
Related Genotype: A/A gri/gri
agouti
Related Genotype: A/A gri/+ or A/A +/?Important Note
This strain is homozygous for the retinal degeneration allele Pde6brd1.Description
On an agouti background gri homozygotes resemble Tyrc-ch homozygotes. There is a graying of the coat due to a lighter than normal phaeomelanin band. There is no change in eye color. gri homozygotes are slightly smaller than their unaffected littermates. Homozygous females breed well, but homozygous males often do not breed. Testis biopsies failed to identify any sperm abnormalities. The gri mutation does not cause a clotting disorder. (Davisson et al., 2000.)Development
gri arose spontaneously in C3H/HeSnJ, generation F163, at The Jackson Laboratory in 1983. It has been maintained by backcross-intercross, breeding homozygous females to C3H/HeSnJ then interbreeding their obligate heterozygous offspring to produce homozygous female breeders. This strain was frozen at N37 in 1997/98.
| Control | ||
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| Untyped from the colony | ||
| Considerations for Choosing Controls | ||
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 Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
gri/gri
C3H/HeSnJ-gri/J
- pigmentation phenotype
- diluted coat color (MGI Ref ID J:60438)
- on an agouti background appearance resembles mice homozygous for the tyrosine allele chinchilla
- the yellow phaeomelanin pigment band on the agouti hairs is lightened to give an overall intense grey coat color
- reproductive system phenotype
- reduced male fertility (MGI Ref ID J:60438)
- males, but not females, exhibit reduced fertility
- no visible sperm abnormalities are seen
- sperm counts were not done
- skin/coat/nails phenotype
- diluted coat color (MGI Ref ID J:60438)
- on an agouti background appearance resembles mice homozygous for the tyrosine allele chinchilla
- the yellow phaeomelanin pigment band on the agouti hairs is lightened to give an overall intense grey coat color
- homeostasis/metabolism phenotype
- *normal* homeostasis/metabolism phenotype (MGI Ref ID J:60438)
- do not appear to exhibit a clotting disorder (assessed by prothrombin time) as is seen in some coat-color-dilution mutants
- growth/size phenotype
- abnormal postnatal growth/weight/body size (MGI Ref ID J:60438)
- abnormal body size (MGI Ref ID J:60438)
- abnormal body weight (MGI Ref ID J:60438)
- decreased body weight (MGI Ref ID J:60438)
- compared to wild-type, mutants weigh less, although not significantly, at 2 weeks and 6 weeks
- decreased body size (MGI Ref ID J:60438)
- visually, mutants appear smaller
- decreased body weight (MGI Ref ID J:60438)
- compared to wild-type, mutants weigh less, although not significantly, at 2 weeks and 6 weeks
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:Pde6brd1 related
gri relatedMouse/Human Gene Homologs
retinitis pigmentosa, autosomal recessive
Sensorineural Research
Retinal Degeneration
Dermatology Research
Color and White Spotting Defects
Developmental Biology Research
Growth Defects
Growth Defects (homozygous)
Reproductive Biology Research
Fertility Defects
males only
| Allele Symbol | gri | ||
|---|---|---|---|
| Allele Name | grey intense | ||
| Allele Type | Spontaneous | ||
| Strain of Origin | C3H/HeSnJ | ||
| Gene Symbol and Name | gri, grey intense | ||
| Chromosome | 11 | ||
| 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
Davisson MT; Johnson KR; Bronson RT; Ward-Bailey PF; Cook SA; Harris BS; Donahue LR. 2000. Grey intense: a new mouse mutation affecting pigmentation. Mamm Genome 11(12):1139-41. [PubMed: 11130986] [MGI Ref ID J:60438]
Colony Maintenance
Diet Information LabDiet® 5K52/5K67
| 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 the retinal degeneration allele Pde6brd1. | |
| Control | ||
|---|---|---|
| Untyped from the colony | ||
| Considerations for Choosing Controls | ||
| USA, Canada and Mexico - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
| International - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
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