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Sluc9O20/A
QTL Variant Detail
Summary
QTL variant: Sluc9O20/A
Name: susceptibility to lung cancer 9; O20/A
MGI ID: MGI:2157049
QTL: Sluc9  Location: Chr8:116828531-116828668 bp  Genetic Position: Chr8, cM position of peak correlated region/allele: 62.82 cM
QTL Note: genome coordinates based on the marker associated with the peak LOD score
Variant
origin
Strain of Specimen:  O20/A
Variant
description
Allele Type:    QTL
Inheritance:    Other (see notes)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Notes
Sluc9 is observed to participate in additive interactions with other Sluc loci.

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

J:50525

The fact that inbred O/20 was more susceptible to lung tumors then Congenic B10.O20 allowed for the mapping of lung tumor genes in OcB Recombinated Congenic strains. Lung tumor size and number could also be assesed by the QTL analysis of F2 mice derived from progenitor O/20 and various OcB strains. Analysis of F2 mice between O/20 and OcB-4 indicated a lung cancer susceptibility gene Sluc9 associated with mouse Chromosome 8 marker D8Mit35.

References
Original:  J:50525 Fijneman RJ, et al., High frequency of interactions between lung cancer susceptibility genes in the mouse: mapping of Sluc5 to Sluc14. Cancer Res. 1998 Nov 1;58(21):4794-8
All:  2 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
12/10/2024
MGI 6.24
The Jackson Laboratory