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Triglq2SM/J
QTL Variant Detail
Summary
QTL variant: Triglq2SM/J
Name: triglyceride QTL 2; SM/J
MGI ID: MGI:2157904
QTL: Triglq2  Location: unknown  Genetic Position: Chr11, Syntenic
Variant
origin
Strain of Specimen:  SM/J
Variant
description
Allele Type:    QTL
Mutation:    Undefined
    This allele confers increased plasma triglyceride levels in male animals compared to A/J. (J:64138)
Inheritance:    Not Specified
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
Notes

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

J:64138

The SMXA (SM/J x A/J) RI line was informative in mapping suggestive QTLs for Body Weight, Insulin, Triglyceride and Phospholipid in selected RI Strains. In female mice a QTL (Triglq2) influencing Triglyceride levels in blood mapped to mouse Chromosome 11 and was associated with D11Rik146.

References
Original:  J:64138 Anunciado RV, et al., Distribution of body weight, blood insulin and lipid levels in the SMXA recombinant inbred strains and the QTL analysis. Exp Anim. 2000 Jul;49(3):217-24
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
03/19/2024
MGI 6.23
The Jackson Laboratory