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Strain Name:

STOCK Oca2p-d/Oca2p-25H/J

Stock Number:

001585

Availability:

Repository-Cryopreserved


Price and Supply Information

General Terms and Conditions

Former Name      STOCK pd/p25H/J    (Changed: 15-DEC-04 )
Genes & Alleles   Oca2;   Oca2p-25H;   Oca2p-d;


Product Information

Strain Details

Type JAX® GEMM® Strain - Mutant Stock
Additional information on JAX® GEMM® Strains.
Type JAX® GEMM® Strain - Radiation Induced Mutation
Specieslaboratory mouse
GenerationF2p

Strain Description
Oca2p-25H/Oca2p-25H mice exhibit significant dilution of coat color with pink eyes, similar in appearance to Oca2p/Oca2p mice. The Oca2p-25H phenotype also includes a slightly jerky gait with some tremor, small body size compared to control littermates, male sterility, female semisterility, and impaired maternal behavior, and the smaller-than-expected proportion of Oca2p-25H homozygous intercross offspring implies reduced prenatal viability (Lyon et al. 1992, Phillips et al, 1977). The Oca2p-25H mutation comprises an inversion of a segment of Chr 7 that alters the 5' end of the Oca2p gene so that no detectable ptranscript is produced, accounting for the pigment-dilution phenotype (Gardner et al. 1992). The deletion also disrupts the Herc2/rjs gene proximal to Oca2p so the transcript sequence diverges from wild-type after the first 8772 bp (of 15 kb in wild-type), resulting in a truncated protein and accounting for the non-pigment related aspects of the Oca2p-25H phenotype (Lehman et al. 1998)(See Mouse Locus Catalog entry for Herc2). Mice homozygous for Oca2p-d are born with lightly pigmented eyes, darker than those of Oca2p/Oca2p mice, which darken by weaning and a coat color "considerably darkerthan that of Oca2p/Oca2p mice, somewhat resembling that of brown [Tyrp1b/Tyrp1b] mice"; both sexes are fertile (Gardner et al. 1977, Lyon et al. 1992). A normal-sized Oca2p transcript is present in eyes of Oca2p-d/Oca2p-d mice (Gardner et al. 1992), and Southern blot analysis revealed no gross alteration of the Oca2p gene (Gardner et al. 1992, Lyon et al. 1992); thus, the molecular nature of the defect is unknown. Oca2p-d/Oca2p-25H compound heterozygotes have a color phenotype intermediate between those of the two homozygotes: eyes are "lighter at birth than those of Oca2p-d/Oca2p-d mice (but not as light as those of Oca2p/Oca2p mice) and darken by weaning"; ears and tail are lighter than those of Oca2p-d/Oca2p-d mice, but coat color is indistinguishable. The compound heterozygotes exhibit no behavioral abnormalities and are fertile (Lyon et al. 1992).

Strain Development
Both the Oca2p-d and Oca2p-25H mutations were radiation induced at the Medical Research Council Radiobiology Unit, Harwell, UK, the former by X-irradiation of the fetus and the latter by neutron irradiation of a male mouse, both of strains/stocks of unidentified lineage.

Gene & Allele Details

Allele Symbol Oca2p-25H
Allele Name pink-eyed 25 Harwell
Common Name(s) Herc2p-25H; p25H;
Gene Symbol and Name Oca2, oculocutaneous albinism II
Chromosome 7
Gene Common Name(s) BEY; BEY1; BEY2; BOCA; D15S12; D7H15S12; D7Icr28RN; D7Nic1; DNA segment, Chr 7, Institute for Cancer Research 28RN; DNA segment, Chr 7, Nicholls 1; DNA segment, Chr 7, human D15S12; EYCL; EYCL2; EYCL3; HCL3; P; PED; SHEP1; p; pink-eyed dilution;
General Note p25H, p-25 Harwell, recessive. This allele was neutron-irradiation-induced. Homozygotes are very similar to p6H homozygotes, except that sperm morphology differs; p25H homozygous males have a lower proportion of normal sperm (J:5219, J:5501, J:15082, J:5808). The sperm shows a loss of negative charge along the whole length of the tail (defined by the inability to stain with the positively charged colloidal iron hydroxide), suggesting that the defect in spermatogenesis mayinvolve the Golgi apparatus and/or plasma membrane (J:11957). Females have reduced fertility. In addition, in p25H homozygotes of both sexes, the pars nervosa of the pituitary contains degenerating nerve axons (J:5508), and the hypothalamus has reduced binding capacity for estradiol-17ß (J:5219). Mutant females can generally produce a small, first litter, but the pups often die neonatally due to poor maternal behavior, which may involve improper nesting (J:49046).
Molecular Note Southern blot analyses using cDNA probes from the pink-eyed dilution locus show that this allele comprises a 5' rearrrangement in the p gene. [MGI Ref ID J:2206]
 
Allele Symbol Oca2p-d
Allele Name dark pink eye
Common Name(s) pd;
Gene Symbol and Name Oca2, oculocutaneous albinism II
Chromosome 7
Gene Common Name(s) BEY; BEY1; BEY2; BOCA; D15S12; D7H15S12; D7Icr28RN; D7Nic1; DNA segment, Chr 7, Institute for Cancer Research 28RN; DNA segment, Chr 7, Nicholls 1; DNA segment, Chr 7, human D15S12; EYCL; EYCL2; EYCL3; HCL3; P; PED; SHEP1; p; pink-eyed dilution;
General Note pd, dark pink eye, recessive. This mutation was probably induced by X-rays. Eyes of homozygotes are slightly pigmented at birth and darken in the next few days; the coat is only slightly diluted. Eyes of pd/p are colorless at birth but darken during the next 2 weeks; the coat is diluted but darker than that of p/p (J:15050). Eyes of pd/pbs are dark at birth; the coat is slightly lighter and the ears slightly darker than those of homozygous pd (J:15082). Female fertility is reduced; males are sterile (J:2108).

Control Information

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Colony Maintenance

Breeding & HusbandryThe male sterility, female semisterility and failure of females to nurture their young that are characteristic of Oca2p-25H homozygotes necessitate maintaining this mutation by mating compound heterozygotes. Oca2p-25H/Oca2p-25H females may produce one or two litters, but the pups must be fostered to survive.

Related Strains

Strains carrying   Oca2p-d allele
000823   STOCK Oca2p-d/Oca2p-6H/J
001747   STOCK Oca2p-d/Oca2p-cp/J
View Strains carrying   Oca2p-d     (2 strains)

View Strains carrying other alleles of Oca2     (23 strains)

Research Applications

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

Oca2p-25H related

Dermatology Research
Color and White Spotting Defects

Endocrine Deficiency Research
Hypothalamus/Pituitary Defects

Mouse/Human Gene Homologs
albinism, oculocutaneous type II, OCA2

Oca2p-d related

Dermatology Research
Color and White Spotting Defects

Mouse/Human Gene Homologs
albinism, oculocutaneous type II, OCA2

Reproductive Biology Research
Fertility Defects

References

Additional References

Price and Supply Information

Strain Name: STOCK Oca2p-d/Oca2p-25H/J
Stock Number: 001585

Price Details

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

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Price(s) in US dollars ($)
Cryorecovery Fee $2470.00

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.

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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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