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Hcs4C3H/He
QTL Variant Detail
Summary
QTL variant: Hcs4C3H/He
Name: hepatocarcinogenesis susceptibility 4; C3H/He
MGI ID: MGI:2155234
QTL: Hcs4  Location: unknown  Genetic Position: Chr2, cM position of peak correlated region/allele: 93.22 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
 
Mutation detailsThis allele confers increased hepatocarcinogenesis susceptibility compared to C57BL/6ByJ and M. spretus. (J:20738)
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:20738

Quantitative trait locus analysis was used to find loci involved in hepatocarcinogenesis susceptibility in 106 male progeny from the (C3H/He x M. spretus)F1 x C57BL/6JBy backcross. One locus, Hcs4, maps to Chromosome 2 in the region of D2Mit25 with a peak LOD score of 3.7 and P = 0.0001.

References
Original:  J:20738 Manenti G, et al., Multiple loci affect genetic predisposition to hepatocarcinogenesis in mice. Genomics. 1994 Sep 1;23(1):118-24
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
04/09/2024
MGI 6.23
The Jackson Laboratory