Search Criteria: Strain Type is "Radiation Induced Mutation"
| Stock Number |
Strain Name Strain Description |
Standard Supply |
| 008684 | B6.Cg-Rag1tm1Mom Tyrp1B-w Tg(Tcra,Tcrb)9Rest/J | Repository- Live |
| These mice are hemizygous for the TRP-1 transgene Tg(Tcra,Tcrb)9Rest, homozygous for the targeted mutation Rag1tm1Mom and homozygous for the white based brown radiation induced mutation of tyrosinase-related protein 1, Tyrp1B-w. These mutant mice express a MHC class II-restricted TCR recognizing the endogenous melanocyte differentiation antigen minimal TRP-1 (tyrosinase-related protein 1) epitope corresponding to amino acids 113 to 127. The transgene is located on the Y chromosome in founder line 9. On a RAG-deficient background, these mice are also homozygous for the Tyrp1B-w mutation and do not produce endogenous tyrosinase-related protein 1. This strain is a source for melanocyte reactive CD4+ cells from antigen-negative animals and may be useful in studies of cancer immunology and therapeutics. | ||
| 005252 | B6EiC3Sn.BLiA-Ts(1716)65Dn/DnJ | Repository- Live |
| Segmentally trisomic Ts(1716)65Dn mice provide a postnatal model for Down syndrome. Ts65Dn mice have three copies of most of the genes on mouse Chromosome 16 that are homologues of human Chromosome 21 genes. These extra genes, along with the centromere and about 5% of proximal Chromosome 17 are contained in a small extra chromosome derived from a reciprocal translocation. The trisomic mice on this genetic background, with the wild-type allele of Pde6b, are similar to the Ts(1716)65Dn trisomic mice (Stock No. 001924) in that they display slightly shorter body length and lower body weight, reduced grip strength, nocturnal hyperactivity, and impaired performance in the Morris water maze. Any differences in the Morris water maze tests for the two genetic backgrounds were found to be very subtle. Distinct from Stock No. 001924, this genetic background is homozygous for the wild-type allele of Pde6b a ..... For more information please see the full phenotype on the strain data sheet | ||
| 008393 | C3H;101-Dync1h1Swl/PopJ | Repository- Live |
| Mice heterozygous for the radiation-induced Sprawling mutation of the cytoplasmic dynein heavy chain 1 gene (Dync1h1Swl) are viable and fertile (the donating investigator reports that less than 50% of males breed successfully). Heterozygous mice display an early-onset hereditary proprioceptive sensory neuropathy with muscle spindle deficiency. Mice are distinguishable around one week after birth by the presence of hindlimb flexion during tail suspension, and around three to four weeks of age develop a typical unsteady gait characterized by jerky and wobbly locomotion. At rest, the hindlimbs are splayed and flexed forward and hindpaws are incapable of gripping structures. Defective proprioception is suggested as proprioceptive sensory neurons are severely compromised in the lumbar dorsal root ganglia of newborns and the H reflex is defective despite normal motor nerve function in the hindlimbs. Homozygous mice die in utero before embryonic day (E)8.5, indicating ..... For more information please see the full phenotype on the strain data sheet | ||
| 000199 | AEJ/GnLeJ | Cryopreserved - Ready for recovery |
| 002306 | B6.Cg-Cdk5rap2an/BrkJ | Cryopreserved - Ready for recovery |
| 002283 | B6.Cg-KitW-19H/EiJ | Cryopreserved - Ready for recovery |
| This deletion is a dominant mutation causing white spotting on the feet, tail, belly, and occasionally elsewhere. Homozygosity is embryonic lethal. On the C57BL/6 background approximately 60% of heterozygous females have a closed vagina. The ovaries from these heterozygotes are normal and fine for transplantation. On the C57BL/6 background in the presence of the YAKR/J Chromosome (available from Stock No. 007250), KitW-19H heterozygosity results in sex reversed XY females. | ||
| 002993 | B6.Cg-KitlSl-18H/EiJ | Cryopreserved - Ready for recovery |
| 001378 | B6;D2-In(3)55Rk Uoxin/J | Cryopreserved - Ready for recovery |
| The Uoxin homozygous phenotype has incomplete penetrance. While 63% of Uoxin homozygotes die by 12-14 days of age, those that live to adulthood generally live a normal breeding life span. Homozygous adults display chronic polyuria, increased serum BUN and creatinine levels, and hydronephrosis with a concomitant inflammatory response that is followed by glomerular and tubular dilation. (Cook et al., 2001.) | ||
| 000125 | B6By.Cg-Sox18Ra Pt Os/J | Cryopreserved - Ready for recovery |
| The Sox18Ra and Sox18Ra-J alleles cause a less severe phenotype than the Sox18Ra-Op allele. The Sox18Ra and Sox18Ra-J alleles are similar mutations and give a very similar phenotype. The Sox18Ra allele has been more broadly described in the literature and will be covered here. Heterozygotes are viable and fertile. Heterozygotes have developmentally retarded sinus hair growth apparent at embryonic day 16.5 and retarded development of pelage follicles apparent by embryonic day 17.5. Thus, heterozygotes have slightly shorter vibrissae evident at birth, and can be distinguished at three days of age by their pink skin which, due to the abnormally sparse development of the coat, fails to darken like that of wildtype siblings. A paucity of fur is apparent by nine days of age and persists throughout life. Compared with the wild type pelage, Sox18Ra/+ coats have longer g ..... For more information please see the full phenotype on the strain data sheet | ||
| 000288 | B6CBACa Aw-J/A-we a Mafbkr/J | Cryopreserved - Ready for recovery |
| 001906 | C3Ga.Cg-Catb/J | Cryopreserved - Ready for recovery |
| 000655 | CBA/CaH-T(14;15)6Ca/J | Cryopreserved - Ready for recovery |
| This strain carries the T(14;15)6Ca translocation which results in nondisjunction at a rate of 4.4% in males and 22.2% in females. CBA/CaH-T6 mice have been used in tandem with the CBA/H strain in foreign body tumorigenesis studies in which the T6 chromosome was used as a marker to distinguish donor cells from host. | ||
| 002503 | ROP/Le-Os Ces1ca/+ Ces1ca/J | Cryopreserved - Ready for recovery |
| This strain originally was maintained segregating for Os and Ces1c, which are approximately 3 cM apart on Chr 8, such that Os and Ces1cb occurred in coupling opposite the wild-type Os allele and Ces1ca. In October 2002, it was discovered that a recombination event between Os and Ces1c had resulted in the strain's becoming fixed for Ces1ca. | ||
| 000269 | SB/LeJ | Cryopreserved - Ready for recovery |
| The SB/Le inbred strain is homozygous for both the satin (Foxq1sa) and beige (Lystbg) mutations. Most of the immunological phenotype is due to the beige mutation. Homozygous mutant beige mice are characterized by a condition that closely resembles Chediak-Higashi disease in man and similar conditions in mink and cattle. Abnormal giant lysosomal granules occur in all tissues with granule-containing cells, including granulocytes, lymphocytes, cells of the liver, kidney, central nervous system, pancreas, and thyroid, and the ducts of most glands; in type II pneumocytes; in mast cells; and in retinal pigment epithelium. Granulocytes from beige mice show defective chemotaxis and reduced bactericidal activity. Beige mice are more susceptible than controls to pneumonitis and to various viral, bacterial, and parasitic infections. They have a severe deficiency of natural killer (NK) cells. Beige mice also have a defective cytotoxic T-cell and cytotoxic antibo ..... For more information please see the full phenotype on the strain data sheet | ||
| 000306 | STOCK Dll3pu + Tyrc-ch/+ Oca2p Tyrc-ch/J | Cryopreserved - Ready for recovery |
| 004711 | STOCK Ednrbs-52Pub | Cryopreserved - Ready for recovery |
| 001610 | STOCK Krt27Re-wc/J | Cryopreserved - Ready for recovery |
| 000109 | STOCK Myo15sh2/J | Cryopreserved - Ready for recovery |
| Mice homozygous for the shaker 2 spontaneous mutation (Myo15sh2) are viable and fertile, showing only a slight reduction in both compared to wildtype mice. Homozygous mutant mice display a phenotype very similar to the behavior and pathology to shaker-1 (Myo7ash1) with the exception that the abnormalities are observed a little earlier in shaker 2 mice. Homozygotes appear to be deaf from the beginning, and the saccular macula is abnormal at birth. The stria vascularis appears normal by light microscopy at 2 weeks, but begins to show degenerative changes shortly thereafter. Many of the cells contain electron-dense inclusions filled with a fine granular material. At 2.5 months, the type I hair cells of the cristae ampullares and maculae utriculi contain rod-shaped inclusion bodies composed of actin filaments. The visible phenotype of the shaker-2 Jackson (Myo15sh2-J, Stock No. 002048<> ..... For more information please see the full phenotype on the strain data sheet | ||
| 001584 | STOCK Oca2p-J/Oca2p-bs/J | Cryopreserved - Ready for recovery |
| Oca2p-J/Oca2p-J mice exhibit significant dilution of coat color with pink eyes, a phenotype similar to that produced by Oca2p/Oca2p. The Oca2p-J mutation is a partial deletion of the gene that completely ablates Oca2p function (Oakey et al. 1996). Oca2p-bs/Oca2p-bs mice show a less extreme coat color dilution and have black eyes from birth; the phenotype of Oca2p-bs homozygotes also includes stunted growth, jerky gait, male sterility, female semisterility, and impaired maternal behavior, and the smaller-than-expected proportion of Oca2p-bs homozygous intercross offspring implies reduced prenatal viability (Lyon et al. 1992). The Oca2p-bs mutation comprises a deletion that begins about 10 kb 5' of the Oca2p locus and extends for about 8 kb in the proximal direc ..... For more information please see the full phenotype on the strain data sheet | ||
| 001585 | STOCK Oca2p-d/Oca2p-25H/J | Cryopreserved - Ready for recovery |
| 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 Chromsome 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 seq ..... For more information please see the full phenotype on the strain data sheet | ||
| 000823 | STOCK Oca2p-d/Oca2p-6H/J | Cryopreserved - Ready for recovery |
| 001747 | STOCK Oca2p-d/Oca2p-cp/J | Cryopreserved - Ready for recovery |
| Mice homozygous for Oca2p-d (dark pink-eye) are born with lightly pigmented eyes, darker than those of Oca2p/Oca2p mice, which darken by weaning and a coat color "considerably darker than 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. Most Oca2p-cp (p-cleft palate, formerly p11H) homozygotes die soon after birth with cleft palate; the few that survive to adulthood exhibit significant dilution of coat co ..... For more information please see the full phenotype on the strain data sheet | ||
| 002307 | WB.Cg-Cdk5rap2an/BrkJ | Cryopreserved - Ready for recovery |
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