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PctmBALB/cAnPt
QTL Variant Detail
Summary
QTL variant: PctmBALB/cAnPt
Name: plasmacytoma modifier; BALB/cAnPt
MGI ID: MGI:3608872
QTL: Pctm  Location: unknown  Genetic Position: Chr1, Syntenic
Variant
origin
Strain of Specimen:  BALB/cAnPt
Variant
description
Allele Type:    QTL
Mutation:    Undefined
    This allele confers resistance to pristane-induced plasmacytomas compared to DBA/2N. (J:15235)
Inheritance:    Recessive
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:15235

Chi square values for mice derived in the intraspecific backcross BALB/cAnPt females x (BALB/cAnPt x DBA/2N)F1 males indicate a potential linkage between Pcts2 and Chromosome 1 marker Fcgr2. Additional markers need to be tested to confirm/reject linkage.

Heterozygosity at Pctm is associated with susceptibility to pristane-induced plasmacytomas, whereas homozygosity for BALB/cAnPt-derived alleles at this locus is associated with resistance.

References
Original:  J:15235 Mock BA, et al., Genetic mapping of tumor susceptibility genes involved in mouse plasmacytomagenesis. Proc Natl Acad Sci U S A. 1993 Oct 15;90(20):9499-503
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
04/16/2024
MGI 6.23
The Jackson Laboratory