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Hcs1C3H/He
QTL Variant Detail
Summary
QTL variant: Hcs1C3H/He
Name: hepatocarcinogenesis susceptibility 1; C3H/He
MGI ID: MGI:2156892
QTL: Hcs1  Location: Chr7:74326121-74326352 bp  Genetic Position: Chr7, cM position of peak correlated region/allele: 43.46 cM
QTL Note: genome coordinates based on the marker associated with the peak LOD score
Variant
origin
Strain of Specimen:  C3H/He
Variant
description
Allele Type:    QTL
Mutation:    Undefined
    This allele confers susceptibility to hepatocarcinogenesis compared to A/J. (J:3657)
Inheritance:    Not Specified
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:3657

Quantitative trait locus analysis (QTL) was used to determine that a locus on mouse Chromosome 7 was associated with liver tumor development in the F2 generation in male A/J x C3H/He mice. There were 174 informative meioses. This locus designated Hsc1 shows a significant association with D7Nds1 and is localized 2 cM distal to Mtv1.

References
Original:  J:3657 Gariboldi M, et al., Chromosome mapping of murine susceptibility loci to liver carcinogenesis. Cancer Res. 1993 Jan 15;53(2):209-11
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