Strain Name: |
B6 x 129S1/SvEi Oca2+ Tyr+-Vsx2or-J/J |
|---|---|
Stock Number: |
000822 |
Availability: | Repository-Cryopreserved |
General Terms and Conditions |
| Former Name |
B6 x 129S1/SvEi p+ Tyr+-Vsx2or-J/J (Changed: 11-FEB-08
) |
|
B6 x 129S1/SvEi p+ Tyr+-Chx10or-J/J (Changed: 29-AUG-07
) | |
|
B6 x 129/SvEi-+p +Tyr-c Chx10or-J (Changed: 15-DEC-04
) | |
| Genes & Alleles | Oca2; Oca2+; Tyr; Tyr+; Vsx2; Vsx2or-J; |
Type JAX® GEMM® Strain - Mutant Stock Additional information on JAX® GEMM® Strains. Species laboratory mouse Generation F58+N1p
Mammalian Phenotype Terms assigned by genotype |
| Allele Symbol | Oca2+ | ||
|---|---|---|---|
| Allele Name | wild type | ||
| 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; | ||
| Allele Symbol | Tyr+ | ||
| Allele Name | wild type | ||
| Gene Symbol and Name | Tyr, tyrosinase | ||
| Chromosome | 7 | ||
| Gene Common Name(s) | C; OCA1A; OCAIA; SHEP3; albino; c; skc35; skin/coat color 35; | ||
| Allele Symbol | Vsx2or-J | ||
| Allele Name | ocular retardation Jackson | ||
| Common Name(s) | Chx10-; orJ; | ||
| Strain of Origin | 129S1/Sv-Oca2<+> Tyr<+> Kitl | ||
| Gene Symbol and Name | Vsx2, visual system homeobox 2 | ||
| Chromosome | 12 | ||
| Gene Common Name(s) | C. elegans ceh-10 homeo domain containing homolog; CHX10; Chx10; HOX10; Hox-10; MCOP2; MCOPCB3; RET1; homeo box 10 cluster; ocular retardation; or; | ||
| General Note | Adult homozygotes resemble adult Chx10or/Chx10or mice. Beginning at 10.5 days of gestation there is much cell death in the normal retina but none in that of Chx10or-J/Chx10or-J mice (J:5966, J:5767). Intercellular channels form in the normal retina and continue along the optic stalk, and the optic nerve grows out of the eye through these channels. Presumably as a result of lack of cell death, the intercellular channels are much reduced in Chx10or-J/Chx10or-J eyes. This may be responsible for absence of the optic nerve (J:6121). Chx10or-J/Chx10or-J homozygotes are fully fertile in both sexes (J:30714). | ||
| Molecular Note | The molecular mutation is a premature stop codon in exon 3, corresponding to the homeobox domain of the encoded protein. [MGI Ref ID J:30800] [MGI Ref ID J:32083] | ||
Strains carrying Oca2+ allele
000090 129S1/Sv-Oca2+ Tyr+ KitlSl-J/J 000091 129T1/Sv-Oca2+ Tyrc-ch Dnd1Ter/J 001279 129T1/Sv-Oca2+ Tyrc-ch-Aft/J 000494 J.Cg-Oca2+ Tyr+ Lystbg/J View Strains carrying Oca2+ (4 strains)
Strains carrying Tyr+ allele
000090 129S1/Sv-Oca2+ Tyr+ KitlSl-J/J 005445 A.B6 Tyr+-Cybanmf333/J 005012 A.B6 Tyr+-Myo5ad-l31J/J 002565 A.B6-Tyr+/J 000899 C.B6-Tyr+ Hbbs/J 000494 J.Cg-Oca2+ Tyr+ Lystbg/J 002281 NFS.C58-Tyr+/J 004304 NOD.CBALs-Tyr+/LtJ View Strains carrying Tyr+ (8 strains)
Strains carrying Vsx2or-J allele
000395 129S1/Sv-Vsx2or-J/J View Strains carrying Vsx2or-J (1 strain)
Strains carrying other alleles of Oca2
000004 ABP/LeJ 000577 B6 x STOCK a Oca2p Hps5ru2 Ednrbs/J 001059 B6By.Cg-Oca2p/J 002460 C3H/HeJ-Oca2p-J Is(7;1)40H/J 000513 C3H/HeJ-Oca2p-J/J 001136 C57BL/6J-Oca2p-un+2J/J 001506 C57BL/6J-Oca2p-un+3J/J 001810 C57BL/6J-Oca2p-un+4J/J 001513 C57BL/6J-Oca2p-un+5J/J 001499 C57BL/6J-Oca2p-un+6J/J 001033 C57BL/6J-Oca2p-un+J/J 000028 C57BL/6J-Oca2p-un/J 000619 FS/EiJ 000306 STOCK Dll3pu + Tyrc-ch/+ Oca2p Tyrc-ch/J 001584 STOCK Oca2p-J/Oca2p-bs/J 001585 STOCK Oca2p-d/Oca2p-25H/J 000823 STOCK Oca2p-d/Oca2p-6H/J 001747 STOCK Oca2p-d/Oca2p-cp/J 001618 STOCK Oca2p/Oca2p Prop1df/J View Strains carrying other alleles of Oca2 (19 strains)
Strains carrying other alleles of Tyr
View Strains carrying other alleles of Tyr (38 strains)
Strains carrying other alleles of Vsx2
001504 NOR2/LtDn-Vsx2or-2J/J View Strains carrying other alleles of Vsx2 (1 strain)
Tyr+ related
Vsx2or-J relatedDermatology Research
Color and White Spotting Defects (oculocutaneous albinism, type I)
Mouse/Human Gene Homologs
albinism, tyrosine negative (wildtype)
non-syndromic microphthalmia, cataracts and iris abnormalities
Sensorineural Research
Eye Defects
| Strain Name: | B6 x 129S1/SvEi Oca2+ Tyr+-Vsx2or-J/J |
| Stock Number: | 000822 |
IMPORTANT NOTE: Prices are based on shipping destination. To view prices, select your shipping destination.
| Standard Supply | Repository-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. |
| Licensing | See General Terms and Conditions below |
Purchasing Information
JAX® Mice Orders
Surgical Services
Contact Information
Orders & Technical Support
Tel: 800.422.6423 or 207.288.5845
Fax: 207.288.6150
Technical Support Email Form