About   Help   FAQ
Nhdlq13B6.129P2-Apoe-tm1Unc/J
QTL Variant Detail
Summary
QTL variant: Nhdlq13B6.129P2-Apoe-tm1Unc/J
Name: non-HDL QTL 13; B6.129P2-Apoetm1Unc/J
MGI ID: MGI:5693293
QTL: Nhdlq13  Location: unknown  Genetic Position: Chr1, Syntenic
Variant
origin
Strain of Specimen:  B6.129P2-Apoetm1Unc/J
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 non-HDL cholesterol level on a Western diet.

QTL Nhdlq13 maps to 54.31 - 82.31 cM on Chromosome 1 with a peak LOD score of 5.93 at 60.31 cM in linkage with non-HDL cholesterol level. C.129P2(B6)-Apoetm1Unc alleles confer increased susceptibility to higher non-HDL cholesterol levels with a dominant 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/23/2024
MGI 6.23
The Jackson Laboratory