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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
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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)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory