About   Help   FAQ
Rv2BALB/cJ
QTL Variant Detail
Summary
QTL variant: Rv2BALB/cJ
Name: Rauscher leukemia virus susceptibility 2; BALB/cJ
MGI ID: MGI:3611350
QTL: Rv2  Location: unknown  Genetic Position: Chr9, Syntenic
Variant
origin
Strain of Specimen:  BALB/cJ
Variant
description
Allele Type:    QTL
Mutation:    Undefined
    This allele confers susceptibility to Rauscher leukemia virus compared to C57BL/6 and C57BL/10. (J:7613)
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Notes

Mapping and Phenotype information for this QTL, its variants and associated markers

J:7613

Rv-2 is assigned to Chromosome 9 by virtue of its typing in two congenic strains, B6.C-H7b/By and B10.C-H7b/(47N)Sn. Both of these strains are congenic for the BALB/cJ alleles at H-7 (59 cM), Mst1r (60 cM; formerly named Fv-2) and Rv-2. The BALB/cJ-derived allele of Rv2 appears to be associated with susceptibility to Rauscher leukemia virus. Additional genetic tests are required to determine whether Rv-2 is identical to Mst1r.

References
Original:  J:7613 Heller E, et al., Chromosomal assignment of two murine genes controlling susceptibility to spleen focus formation by Rauscher leukemia virus. Exp Hematol. 1984 Sep;12(8):645-9
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
11/12/2024
MGI 6.24
The Jackson Laboratory