About   Help   FAQ
Vsx2or-2J
Spontaneous Allele Detail
Summary
Symbol: Vsx2or-2J
Name: visual system homeobox 2; ocular retardation 2 Jackson
MGI ID: MGI:1856113
Gene: Vsx2  Location: Chr12:84616602-84642231 bp, + strand  Genetic Position: Chr12, 39.28 cM
Alliance: Vsx2or-2J page
Mutation
origin
Strain of Origin:  NOR/LtDn
Mutation
description
Allele Type:    Spontaneous
Inheritance:    Recessive
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Vsx2 Mutation:  23 strains or lines available
Notes
A remutation at the Chx10 locus occurred in NOR/LtDn, a genetically contaminated subline of the nonobese diabetic NOD/Lt strain. Eye phenotypes in homozygotes resemble the eye abnormalities reported in Chx10or-J/Chx10or-J homozygotes. NOR-Chx10or-2J/Chx10or-2J homozygotes of both sexes are infertile and show defective germ cell maturation. Chx10or-J/Chx10or-2J heterozygotes are fully fertile in both sexes (J:30714).
References
Original:  J:30714 Prochazka M, et al., or-2J; a new remutation at ocular retardation (or) associated with sterility. Mouse Genome. 1990;87:93
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
10/29/2024
MGI 6.24
The Jackson Laboratory