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Cath3C.129P2(B6)-Apoe-tm1Unc
QTL Variant Detail
Summary
QTL variant: Cath3C.129P2(B6)-Apoe-tm1Unc
Name: carotid atherosclerosis 3; C.129P2(B6)-Apoetm1Unc
MGI ID: MGI:5689922
QTL: Cath3  Location: unknown  Genetic Position: Chr13, Syntenic
Variant
origin
Strain of Specimen:  C.129P2(B6)-Apoetm1Unc
Variant
description
Allele Type:    QTL
Inheritance:    Not Specified
Notes

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

J:197549

Linkage analysis was performed on 266 female (B6.129P2-Apoetm1Unc/J x C.129P2(B6)-Apoetm1Unc)F2 intercross mice using 130 SNP markers to identify QTL associated with susceptibility to athleroscotic carotid lesion. QTL mapping was performed using a nonparametric method.

QTL Cath3 maps to 18.99 - 59.69 cM on Chromosome 13 with a peak LOD score of 4.292 at 48.99 cM in linkage with athleroscotic carotid lesion incidence. B6.129P2-Apoetm1Unc/J alleles confer increased susceptibility to athleroscotic carotid lesion with an additive mode of inheritance.

References
Original:  J:197549 Rowlan JS, et al., New quantitative trait loci for carotid atherosclerosis identified in an intercross derived from apolipoprotein E-deficient mouse strains. Physiol Genomics. 2013 Apr 16;45(8):332-42
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
05/21/2024
MGI 6.23
The Jackson Laboratory